Canonical Allele Identifier: PA2829478345
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 1897995
ClinVar RCV Id: RCV002573714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Thr64Ser
CA2706509
NM_004122.2:c.190A>T
CA355516224
NM_004122.2:c.191C>G