Canonical Allele Identifier: PA2826832946
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 576536
ClinVar RCV Id: RCV000699052 RCV003303169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Thr1063Met
CA2320325
NM_001293306.2:c.3188C>T