Canonical Allele Identifier: PA1139671319
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 871085
ClinVar RCV Id: RCV001090855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Pro440Ala
CA346480443
NM_001029883.3:c.1318C>G