Canonical Allele Identifier: PA265747
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67951
ClinVar RCV Id: RCV000058736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser1672Tyr
CA018848
NM_198056.3:c.5015C>A