Canonical Allele Identifier: PA916021563
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 436247
ClinVar RCV Id: RCV000501156
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Thr895Ile
CA10079154
NM_001315529.2:c.2684C>T