Canonical Allele Identifier: PA2830433319
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3073972
ClinVar RCV Id: RCV004012514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Thr1893Ile
CA352140350
NM_198056.3:c.5678C>T