Canonical Allele Identifier: PA2825494728
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774465
ClinVar RCV Id: RCV003592348

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asp953Gly
CA352140504
NM_001099405.2:c.2858A>G