Canonical Allele Identifier: PA109662
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_006454.1:p.Arg38Cys
CA263227
NM_006463.6:c.112C>T