Canonical Allele Identifier: PA2826951582
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 159589
ClinVar RCV Id: RCV000147114 RCV000365165 RCV001682854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Arg1045Cys
CA172994
NM_001315529.2:c.3133C>T