Allele Registry

Canonical Allele Identifier: PA658664741

Gene: CRTAP HGNC NCBI

ClinVar Allele:

452331

ClinVar RCV:

RCV000540867

ClinVar Variation:

465814

HGVS (amino-acid)	Matching Registered Transcripts
NP_006362.1:p.Gly219Ser	CA2300355 NM_006371.5:c.655G>A