Canonical Allele Identifier: PA1139672032
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 860176
ClinVar RCV Id: RCV001066440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Arg1197Ser
CA346472846
NM_001029883.3:c.3589C>A