Canonical Allele Identifier: PA2825130921
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 629164
ClinVar RCV Id: RCV001841914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Pro1186Gln
CA062038
NM_000335.5:c.3557C>A