Canonical Allele Identifier: PA174023
Gene: GHRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 161436
ClinVar RCV Id: RCV000148941 RCV003992197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000814.2:p.Arg94Gln
CA174022
NM_000823.4:c.281G>A