Canonical Allele Identifier: PA113046
Gene: PTH HGNC NCBI
ClinVar RCV:
RCV000014766
ClinVar Variation:
13758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000306.1:p.Ser23Pro
CA123437
NM_000315.4:c.67T>C