Canonical Allele Identifier: PA2825496077
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67880
ClinVar RCV Id: RCV000058660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Pro1420Leu
CA018135
NM_001099405.2:c.4259C>T