Allele Registry

Canonical Allele Identifier: PA916021762

Gene: PTH HGNC NCBI

ClinVar RCV:

RCV000014764

ClinVar Variation:

13756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001303281.1:p.Cys50Arg	CA123436 NM_001316352.2:c.148T>C