Canonical Allele Identifier: PA2825942573
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 859644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp1757Asn
CA064352
NM_001160160.2:c.5269G>A