Canonical Allele Identifier: PA1139671266
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 859800
ClinVar RCV Id: RCV001065990

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Asp411Glu
CA346480617
NM_001029883.3:c.1233C>G
CA346480618
NM_001029883.3:c.1233C>A