Canonical Allele Identifier: PA645427444
Gene: CRTAP HGNC NCBI

Linked Data

ClinVar Variation Id: 289670
ClinVar RCV Id: RCV000263295 RCV002518097
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006362.1:p.Gly7Ala
CA10606514
NM_006371.5:c.20G>C