Canonical Allele Identifier: PA645435765
Gene: PCARE HGNC NCBI

Linked Data

ClinVar Variation Id: 335641
ClinVar RCV Id: RCV000393942 RCV001044077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025054.1:p.Arg1177Trp
CA1591905
NM_001029883.3:c.3529C>T