Canonical Allele Identifier: PA2825492648
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1982034
ClinVar RCV Id: RCV003776931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Asn288Lys
CA352150475
NM_001099405.2:c.864C>A
CA352150477
NM_001099405.2:c.864C>G