Canonical Allele Identifier: PA153190
Gene: CRPPA HGNC NCBI

Linked Data

ClinVar Variation Id: 129286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001094896.1:p.Pro11Arg
CA153189
NM_001101426.4:c.32C>G