Allele Registry

Canonical Allele Identifier: PA113032

Gene: PTH HGNC NCBI

ClinVar RCV:

RCV000014764

ClinVar Variation:

13756

HGVS (amino-acid)	Matching Registered Transcripts
NP_000306.1:p.Cys18Arg	CA123436 NM_000315.4:c.52T>C