Canonical Allele Identifier: PA1139704997
Gene: GNB3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002066.1:p.Asp27Gly
CA383671466
NM_002075.4:c.80A>G