Allele Registry

Canonical Allele Identifier: PA2825375675

Gene: PTCHD3 HGNC NCBI

ClinVar RCV:

RCV004071381

ClinVar Variation:

2206983

HGVS (amino-acid)	Matching Registered Transcripts
NP_001030014.2:p.Asp218Gly	CA376389682 NM_001034842.5:c.653A>G