Canonical Allele Identifier: PA216059
Gene: PTH1R HGNC NCBI

Linked Data

ClinVar Variation Id: 64398
ClinVar RCV Id: RCV000054585 RCV001144123 RCV001144124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000307.1:p.Thr435Met
CA216058
NM_000316.3:c.1304C>T