Canonical Allele Identifier: PA2825940290
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2819859
ClinVar RCV Id: RCV003706483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Phe272Leu
CA352150660
NM_001160160.2:c.816C>A
CA352150662
NM_001160160.2:c.816C>G
CA352150671
NM_001160160.2:c.814T>C