Canonical Allele Identifier: PA645505431
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 406416

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Met1214Thr
CA16611463
NM_198056.3:c.3641T>C