Canonical Allele Identifier: PA115597
Gene: NIPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2521
ClinVar RCV Id: RCV000002629
ClinVar Variation Id: 2523
ClinVar RCV Id: RCV000002631 RCV000516051 RCV000713477 RCV001003981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135747.1:p.Gly31Arg
CA115593
NM_001142275.1:c.91G>C
CA115595
NM_001142275.1:c.91G>A