Canonical Allele Identifier: PA335927
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 216841
ClinVar RCV Id: RCV000498992 RCV001842951 RCV003539815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Tyr1949Cys
CA335923
NM_000335.5:c.5846A>G