Canonical Allele Identifier: PA2827791006
Gene: STAMBP HGNC NCBI

Linked Data

ClinVar Variation Id: 1467635
ClinVar RCV Id: RCV001966474
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001340896.1:p.Thr351Ser
CA1717696
NM_001353967.2:c.1052C>G
CA347293333
NM_001353967.2:c.1051A>T