Canonical Allele Identifier: PA658655261
Gene: POC1B HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_758440.1:p.Leu439Pro
CA385985019
NM_172240.3:c.1316T>C