Canonical Allele Identifier: PA2825131155
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2772407
ClinVar RCV Id: RCV003576684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Ala1293Asp
CA72945858
NM_000335.5:c.3878C>A