Canonical Allele Identifier: PA314902
Gene: GOSR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 205630
ClinVar RCV Id: RCV000187615 RCV001408579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004278.2:p.Leu130Phe
CA314901
NM_004287.5:c.388C>T