Canonical Allele Identifier: PA1139755679
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 963612
ClinVar RCV Id: RCV001237661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly268Cys
CA352150709
NM_198056.3:c.802G>T