Canonical Allele Identifier: PA645435744
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 335642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Ser1015Tyr
CA1592042
NM_001029883.3:c.3044C>A