Allele Registry

Canonical Allele Identifier: PA2826201762

Gene: GPR35 HGNC NCBI

ClinVar RCV:

RCV001621548

ClinVar Variation:

1234784

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182311.1:p.Thr139Met	CA2206242 NM_001195382.3:c.416C>T