Canonical Allele Identifier: PA2580133469
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 1970021
ClinVar RCV Id: RCV002730328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Leu1184Val
CA346472926
NM_001029883.3:c.3550C>G