Canonical Allele Identifier: PA2580558099
Gene: GHSR HGNC NCBI
ClinVar RCV:
RCV002827509
ClinVar Variation:
2279034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940799.1:p.Leu314Phe
CA355512091
NM_198407.2:c.940C>T