Canonical Allele Identifier: PA2827791167
Gene: STAMBP HGNC NCBI

Linked Data

ClinVar Variation Id: 50791
ClinVar RCV Id: RCV000043572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340898.1:p.Glu42Gly
CA263222
NM_001353969.2:c.125A>G