Canonical Allele Identifier: PA2825495994
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2742353
ClinVar RCV Id: RCV003557938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu1387Phe
CA062892
NM_001099405.2:c.4161G>C
CA352146637
NM_001099405.2:c.4161G>T