Canonical Allele Identifier: PA200626
Gene: NIPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193496
ClinVar RCV Id: RCV000173569 RCV000228668 RCV000368522 RCV000516128 RCV001697203
ClinVar Variation Id: 1474382
ClinVar RCV Id: RCV001971233
ClinVar Variation Id: 2975138
ClinVar RCV Id: RCV003830744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653200.2:p.Ala15_Ala16dup
CA200624
NM_144599.5:c.42_47dup
CA2627249194
NM_144599.5:c.47_48insGGCAGC
CA2730476343
NM_144599.5:c.44_45insAGCGGC