Canonical Allele Identifier: PA2825945202
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 3070379
ClinVar RCV Id: RCV004011897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153633.1:p.Val1493Leu
CA352143948
NM_001160161.2:c.4477G>T
CA352143949
NM_001160161.2:c.4477G>C