Canonical Allele Identifier: PA2829478388
Gene: GHSR HGNC NCBI

Linked Data

ClinVar Variation Id: 3099745
ClinVar RCV Id: RCV004390570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004113.1:p.Ala144Val
CA355514507
NM_004122.2:c.431C>T