Canonical Allele Identifier: PA174805
Gene: GPR82 HGNC NCBI

Linked Data

ClinVar Variation Id: 161798
ClinVar RCV Id: RCV000149334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_543007.1:p.Gly161Val
CA174804
NM_080817.5:c.482G>T