Allele Registry

Canonical Allele Identifier: PA2829478407

Gene: GHSR HGNC NCBI

ClinVar Allele:

1330634

ClinVar RCV:

RCV001824197

RCV002246538

ClinVar Variation:

1339488

HGVS (amino-acid)	Matching Registered Transcripts
NP_004113.1:p.Val182Ala	CA87785335 NM_004122.2:c.545T>C