Canonical Allele Identifier: PA2827921447
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala185Thr
CA019331
NM_001354701.2:c.553G>A