Canonical Allele Identifier: PA2826247740
Gene: POC1B HGNC NCBI

Linked Data

ClinVar Variation Id: 155770
ClinVar RCV Id: RCV000143863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186706.1:p.Gln25del
CA170704
NM_001199777.2:c.73_75del
CA385993830
NM_001199777.2:c.73C>T