Canonical Allele Identifier: PA2830471339
Gene: STAMBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1298814
ClinVar RCV Id: RCV001727144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_964010.1:p.Tyr63Cys
CA1717451
NM_201647.4:c.188A>G