Canonical Allele Identifier: PA2826952056
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 436202
ClinVar RCV Id: RCV000502860 RCV001857142 RCV003424063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Val1776Ile
CA10080059
NM_001315529.2:c.5326G>A