Allele Registry

Canonical Allele Identifier: PA117155

Gene: CRTAP HGNC NCBI

ClinVar Allele:

19990

ClinVar RCV:

RCV000005239

RCV002468961

ClinVar Variation:

4951

HGVS (amino-acid)	Matching Registered Transcripts
NP_006362.1:p.Met1Ile