Canonical Allele Identifier: PA2825943599
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3074077
ClinVar RCV Id: RCV004012619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met438Leu
CA352148400
NM_001160161.2:c.1312A>T
CA352148403
NM_001160161.2:c.1312A>C