Canonical Allele Identifier: PA216061
Gene: PTH1R HGNC NCBI

Linked Data

ClinVar Variation Id: 64399
ClinVar RCV Id: RCV000054586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000307.1:p.Arg106Cys
CA216060
NM_000316.3:c.316C>T