Canonical Allele Identifier: PA2499303313
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 999632
ClinVar RCV Id: RCV003656785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Phe1928Val
CA352139966
NM_198056.3:c.5782T>G