Canonical Allele Identifier: PA915995808
Gene: PTH1R HGNC NCBI

Linked Data

ClinVar Variation Id: 13743
ClinVar RCV Id: RCV000014750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171673.1:p.Thr410Pro
CA123422
NM_001184744.1:c.1228A>C