Canonical Allele Identifier: PA915995778
Gene: PTH1R HGNC NCBI
ClinVar RCV:
RCV000054586
ClinVar Variation:
64399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171673.1:p.Arg106Cys
CA216060
NM_001184744.1:c.316C>T