Canonical Allele Identifier: PA2826247815
Gene: POC1B HGNC NCBI
ClinVar RCV:
RCV001207359
ClinVar Variation:
938183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186706.1:p.Gly226Arg
CA6714404
NM_001199777.2:c.676G>A
CA385995721
NM_001199777.2:c.676G>C