Canonical Allele Identifier: PA2573313933
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1509648
ClinVar RCV Id: RCV003773407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Trp195Arg
CA352153586
NM_198056.3:c.583T>A
CA352153588
NM_198056.3:c.583T>C