Canonical Allele Identifier: PA645435768
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 335639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Gly1220Ser
CA1591870
NM_001029883.3:c.3658G>A