Canonical Allele Identifier: PA236827
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 191504
ClinVar RCV Id: RCV000171703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Met273Thr
CA019816
NM_198056.3:c.818T>C