Canonical Allele Identifier: PA2825132872
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 520462
ClinVar RCV Id: RCV000622370 RCV001143899 RCV001143900 RCV001143901 RCV001143902 RCV001143898 RCV001145795 RCV001841808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Val1979Phe
CA065024
NM_000335.5:c.5935G>T