Canonical Allele Identifier: PA2825942962
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 1377908
ClinVar RCV Id: RCV003657374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153632.1:p.Val1983_Ter1984insLeuAlaSerAlaTrpLeuAlaArgThrHis
CA352138958
NM_001160160.2:c.5951G>T