Canonical Allele Identifier: PA2827791027
Gene: STAMBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1412908
ClinVar RCV Id: RCV001925604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340897.1:p.Pro10Leu
CA1717423
NM_001353968.2:c.29C>T