ClinGen Allele Registry
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Canonical Allele Identifier:
PA916005642
Gene: GHR
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
23676
ClinVar RCV:
RCV000009169
RCV000660368
RCV000723957
RCV000764609
RCV001156022
RCV003398475
RCV003478972
ClinVar Variation:
8637
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001229328.1:p.Arg186Cys
CA119799
NM_001242399.2:c.556C>T