Canonical Allele Identifier: PA173139
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 159686
ClinVar RCV Id: RCV000147238 RCV000972985 RCV001001877
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006022.3:p.Thr3005Met
CA173138
NM_006031.5:c.9014C>T