Canonical Allele Identifier: PA2826952797
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 197441
ClinVar RCV Id: RCV000178469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Leu2852Pro
CA245581
NM_001315529.2:c.8555T>C