Canonical Allele Identifier: PA108084
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Leu1501Val
CA018357
NM_198056.3:c.4501C>G