Canonical Allele Identifier: PA2825131164
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3072091
ClinVar RCV Id: RCV004012121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Met1295Leu
CA352148202
NM_000335.5:c.3883A>T
CA352148204
NM_000335.5:c.3883A>C