Canonical Allele Identifier: PA2573314009
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1476979
ClinVar RCV Id: RCV003657567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.His1204Gln
CA352138091
NM_198056.3:c.3612C>G
CA352138092
NM_198056.3:c.3612C>A