Canonical Allele Identifier: PA107967
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 9386
ClinVar RCV Id: RCV000009984 RCV000058427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_932173.1:p.Gly514Cys
CA014960
NM_198056.3:c.1540G>T