Canonical Allele Identifier: PA645399401
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 287397
ClinVar RCV Id: RCV000286792 RCV000726003 RCV000765510 RCV003910001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006022.3:p.Ala1952Val
CA10080102
NM_006031.5:c.5855C>T