Canonical Allele Identifier: PA1139755734
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 858024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Leu306Val
CA065896
NM_198056.3:c.916C>G