Canonical Allele Identifier: PA645435740
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 335644

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Pro989Ala
CA1592068
NM_001029883.3:c.2965C>G