Canonical Allele Identifier: PA2825942574
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Asp1757Gly
CA019174
NM_001160160.2:c.5270A>G