Canonical Allele Identifier: PA2580555141
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1969698
ClinVar RCV Id: RCV003658090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Pro54Leu
CA352158449
NM_198056.3:c.161C>T