Canonical Allele Identifier: PA916005617
Gene: GHR HGNC NCBI

Linked Data

ClinVar Variation Id: 492773
ClinVar RCV Id: RCV000581563 RCV002469211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229328.1:p.Trp129Arg
CA359695204
NM_001242399.2:c.385T>A
CA359695205
NM_001242399.2:c.385T>C