Canonical Allele Identifier: PA2499274199
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1176456
ClinVar RCV Id: RCV001531997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Gly540Cys
CA352167378
NM_006514.4:c.1618G>T