Canonical Allele Identifier: PA2573177637
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 1511784
ClinVar RCV Id: RCV002020590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Ser437del
CA767532904
NM_001029883.3:c.1306_1308del