Canonical Allele Identifier: PA2830471482
Gene: STAMBP HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_964010.1:p.Thr351Ser
CA1717696
NM_201647.4:c.1052C>G
CA347293333
NM_201647.4:c.1051A>T