Allele Registry

Canonical Allele Identifier: PA916021763

Gene: PTH HGNC NCBI

ClinVar RCV:

RCV000014766

ClinVar Variation:

13758

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