Canonical Allele Identifier: PA1139734412
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 853573
ClinVar RCV Id: RCV001058409
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Tyr1482del
CA1943868
NM_001365536.1:c.4444_4446del