Canonical Allele Identifier: PA2742029268
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2774470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Met741Leu
CA352144506
NM_198056.3:c.2221A>C
CA352144508
NM_198056.3:c.2221A>T