Canonical Allele Identifier: PA221088
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93216
ClinVar RCV Id: RCV000079079
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Phe124del
CA221087
NM_000528.4:c.371_373del