Canonical Allele Identifier: PA2826247889
Gene: POC1B HGNC NCBI
ClinVar RCV:
RCV000513570
ClinVar Variation:
444304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186706.1:p.Leu397Pro
CA385985019
NM_001199777.2:c.1190T>C