Canonical Allele Identifier: PA2826952770
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 159686
ClinVar RCV Id: RCV000147238 RCV000972985 RCV001001877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Thr2808Met
CA173138
NM_001315529.2:c.8423C>T