Canonical Allele Identifier: PA199810
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67713
ClinVar RCV Id: RCV000058480 RCV000171571 RCV000182996 RCV000619698 RCV001842311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Pro701Leu
CA015838
NM_198056.3:c.2102C>T