Canonical Allele Identifier: PA658678755
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 463350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Tyr1889Cys
CA72937852
NM_198056.3:c.5666A>G