Canonical Allele Identifier: PA2825129695
Gene: SCN5A HGNC NCBI

Linked Data

ClinVar Variation Id: 2977377
ClinVar RCV Id: RCV003831495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000326.2:p.Gln660His
CA352145037
NM_000335.5:c.1980G>T
CA352145038
NM_000335.5:c.1980G>C