Canonical Allele Identifier: PA2825942148
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67895
ClinVar RCV Id: RCV000058675 RCV002223185 RCV001842364 RCV002490660 RCV004019051
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Met1486Leu
CA018283
NM_001160160.2:c.4456A>C
CA352144358
NM_001160160.2:c.4456A>T