Canonical Allele Identifier: PA2827923835
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Asp1771Gly
CA019174
NM_001354701.2:c.5312A>G