Allele Registry

Canonical Allele Identifier: PA103695

Gene: GPR143 HGNC NCBI

ClinVar RCV:

RCV000011268

ClinVar Variation:

10522

HGVS (amino-acid)	Matching Registered Transcripts
NP_000264.2:p.Ser89Phe	CA121108 NM_000273.3:c.266C>T