Canonical Allele Identifier: PA2825941234
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Met907Ile
CA352141527
NM_001160160.2:c.2721G>T
CA352141528
NM_001160160.2:c.2721G>C
CA352141529
NM_001160160.2:c.2721G>A