Canonical Allele Identifier: PA278921
Gene: GOSR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 208982
ClinVar RCV Id: RCV000190901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004278.2:p.Lys164del
CA278920
NM_004287.5:c.491_493del
CA400018886
NM_004287.5:c.487A>T
CA400018897
NM_004287.5:c.490A>T