Canonical Allele Identifier: PA1139763056
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 922050
ClinVar RCV Id: RCV001843110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Ser1920Ala
CA352140059
NM_198056.3:c.5758T>G