Allele Registry

Canonical Allele Identifier: PA2829197708

Gene: CRTAP HGNC NCBI

ClinVar RCV:

RCV000540867

ClinVar Variation:

465814

HGVS (amino-acid)	Matching Registered Transcripts
NP_001380294.1:p.Gly169Ser	CA2300355 NM_001393365.1:c.505G>A