Canonical Allele Identifier: PA916021763
Gene: PTH HGNC NCBI
ClinVar RCV:
RCV000014766
ClinVar Variation:
13758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303281.1:p.Ser55Pro
CA123437
NM_001316352.2:c.163T>C