Canonical Allele Identifier: PA2825492059
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1171546
ClinVar RCV Id: RCV001842094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Lys91Asn
CA352157699
NM_001099405.2:c.273G>T
CA352157701
NM_001099405.2:c.273G>C