Canonical Allele Identifier: PA2829665871
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_006454.1:p.Thr351Ser
CA1717696
NM_006463.6:c.1052C>G
CA347293333
NM_006463.6:c.1051A>T