Canonical Allele Identifier: PA265022
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 67708
ClinVar RCV Id: RCV000058475 RCV001842307 RCV003764735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Cys683Gly
CA015785
NM_198056.3:c.2047T>G