Canonical Allele Identifier: PA265967
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 68056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Val300Ile
CA019931
NM_198056.3:c.898G>A