Canonical Allele Identifier: PA2825944329
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2837300
ClinVar RCV Id: RCV003692487

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Leu938Val
CA352140720
NM_001160161.2:c.2812C>G