Canonical Allele Identifier: PA2826952705
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 895965
ClinVar RCV Id: RCV001138352 RCV002556948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Arg2727His
CA10081085
NM_001315529.2:c.8180G>A