Canonical Allele Identifier: PA1139672079
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 898961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Thr1207Asn
CA1591878
NM_001029883.3:c.3620C>A