Canonical Allele Identifier: PA107745
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9400
ClinVar RCV Id: RCV000010002 RCV000022945 RCV000058552 RCV000469648 RCV000755695 RCV001528558 RCV001841242 RCV002321478 RCV004526592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Glu1053Lys
CA016871
NM_198056.3:c.3157G>A