Canonical Allele Identifier: PA2827923110
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 947395
ClinVar RCV Id: RCV001218463
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341630.1:p.Pro1309Ser
CA352148124
NM_001354701.2:c.3925C>T