Canonical Allele Identifier: PA113631
Gene: STT3A HGNC NCBI

Linked Data

ClinVar Variation Id: 102443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265432.1:p.Val626Ala
CA249894
NM_001278503.2:c.1877T>C