Canonical Allele Identifier: PA1139705182
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_006022.3:p.Arg2924His
CA10081085
NM_006031.5:c.8771G>A