Allele Registry

Canonical Allele Identifier: PA2573101103

Gene: GHSR HGNC NCBI

ClinVar Allele:

1330634

ClinVar RCV:

RCV001824197

RCV002246538

ClinVar Variation:

1339488

HGVS (amino-acid)	Matching Registered Transcripts
NP_940799.1:p.Val182Ala	CA87785335 NM_198407.2:c.545T>C