Canonical Allele Identifier: PA2825945545
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 519384
ClinVar Variation Id: 2027600
ClinVar RCV Id: RCV003658312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Met1712Ile
CA352141596
NM_001160161.2:c.5136G>A
CA352141598
NM_001160161.2:c.5136G>T
CA352141600
NM_001160161.2:c.5136G>C