Canonical Allele Identifier: PA2827790923
Gene: STAMBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1298814
ClinVar RCV Id: RCV001727144
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340896.1:p.Tyr63Cys
CA1717451
NM_001353967.2:c.188A>G