Canonical Allele Identifier: PA2825497617
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3069459
ClinVar RCV Id: RCV004008003

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Ser1948Pro
CA352139533
NM_001099405.2:c.5842T>C