Canonical Allele Identifier: PA200356
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 193135
ClinVar Variation Id: 193142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Gln1020Arg
CA200355
NM_001029883.3:c.3058_3059delinsAG
CA238641
NM_001029883.3:c.3059A>G