Allele Registry

Canonical Allele Identifier: PA2829597958

Gene: GPR35 HGNC NCBI

ClinVar RCV:

RCV001621548

ClinVar Variation:

1234784

HGVS (amino-acid)	Matching Registered Transcripts
NP_005292.2:p.Thr108Met	CA2206242 NM_005301.5:c.323C>T