Canonical Allele Identifier: PA2827923851
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9382
ClinVar RCV Id: RCV000009979 RCV000009980 RCV001530164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Tyr1776_Glu1777insAsp
CA025554
NM_001354701.2:c.5328_5330dup