Canonical Allele Identifier: PA2828583771
Gene: GABRG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1685837
ClinVar RCV Id: RCV002250004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362276.1:p.Thr281Ser
CA362182305
NM_001375347.1:c.841A>T
CA362182310
NM_001375347.1:c.842C>G