Allele Registry

Canonical Allele Identifier: PA2580251152

Gene: PTCHD3 HGNC NCBI

ClinVar RCV:

RCV004071381

ClinVar Variation:

2206983

HGVS (amino-acid)	Matching Registered Transcripts
NP_001382672.1:p.Asp218Gly	CA376389682 NM_001395743.1:c.653A>G