Canonical Allele Identifier: PA915995816
Gene: PTH1R HGNC NCBI

Linked Data

ClinVar Variation Id: 13747
ClinVar RCV Id: RCV000014754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171673.1:p.Ile458Arg
CA123426
NM_001184744.1:c.1373T>G