Canonical Allele Identifier: PA2825940990
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9391
ClinVar RCV Id: RCV000009989 RCV000058488 RCV003654175 RCV003591627 RCV003996084
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Ala735Val
CA015951
NM_001160160.2:c.2204C>T