ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826298750
Gene: GHR
HGNC
NCBI
Linked Data
ClinVar Variation Id:
8632
ClinVar RCV Id:
RCV000009164
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001229328.1:p.Phe121Ser
CA119790
NM_001242399.2:c.362T>C