Canonical Allele Identifier: PA915995818
Gene: PTH1R HGNC NCBI

Linked Data

ClinVar Variation Id: 345598
ClinVar RCV Id: RCV000309388 RCV000350211 RCV003765997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171673.1:p.Arg476His
CA2359562
NM_001184744.1:c.1427G>A