Canonical Allele Identifier: PA2825538487
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2959874
ClinVar RCV Id: RCV003812049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092874.1:p.Asn958Lys
CA72926407
NM_001099404.2:c.2874C>A
CA352140418
NM_001099404.2:c.2874C>G