Canonical Allele Identifier: PA916021762
Gene: PTH HGNC NCBI

Linked Data

ClinVar Variation Id: 13756
ClinVar RCV Id: RCV000014764

Amino-acid Alleles

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