Canonical Allele Identifier: PA245582
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_006022.3:p.Leu3049Pro
CA245581
NM_006031.5:c.9146T>C