Canonical Allele Identifier: PA2825492709
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 858024
ClinVar RCV Id: RCV001063819 RCV001552115 RCV004000137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001092875.1:p.Leu306Val
CA065896
NM_001099405.2:c.916C>G