Canonical Allele Identifier: PA1139763052
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 919820
ClinVar RCV Id: RCV001842721 RCV002348606 RCV003542329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Arg1919His
CA064762
NM_198056.3:c.5756G>A