Canonical Allele Identifier: PA1139753873
Gene: NIPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 887002
ClinVar RCV Id: RCV001119480 RCV003227915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653200.2:p.Gly17Arg
CA7426226
NM_144599.5:c.49G>C
CA391298355
NM_144599.5:c.49G>A