Canonical Allele Identifier: PA2825131808
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1467082
ClinVar RCV Id: RCV003773017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Leu1578Pro
CA352143730
NM_000335.5:c.4733T>C