Canonical Allele Identifier: PA645398314
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 436172
ClinVar RCV Id: RCV000500184 RCV002524249 RCV002506228 RCV004023394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006022.3:p.Asp47His
CA10078149
NM_006031.5:c.139G>C