Canonical Allele Identifier: PA2499303285
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1299964
ClinVar RCV Id: RCV001730414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Phe733Leu
CA059897
NM_198056.3:c.2199C>G
CA72932536
NM_198056.3:c.2199C>A
CA352144561
NM_198056.3:c.2197T>C