Canonical Allele Identifier: PA330077
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67895

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Met1487Leu
CA018283
NM_198056.3:c.4459A>C
CA352144358
NM_198056.3:c.4459A>T