Canonical Allele Identifier: PA113032
Gene: PTH HGNC NCBI

Linked Data

ClinVar Variation Id: 13756
ClinVar RCV Id: RCV000014764

Amino-acid Alleles

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