Canonical Allele Identifier: PA263228
Gene: STAMBP HGNC NCBI

Linked Data

ClinVar Variation Id: 50793
ClinVar RCV Id: RCV000043574 RCV000426675
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_964010.1:p.Arg38Cys
CA263227
NM_201647.4:c.112C>T