Canonical Allele Identifier: PA2827923597
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1006492
ClinVar RCV Id: RCV003656815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Ala1621Thr
CA72938309
NM_001354701.2:c.4861G>A