Canonical Allele Identifier: PA915995779
Gene: PTH1R HGNC NCBI

Linked Data

ClinVar Variation Id: 13745
ClinVar RCV Id: RCV000014752 RCV002482867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171673.1:p.Pro132Leu
CA123425
NM_001184744.1:c.395C>T