Canonical Allele Identifier: PA2741843714
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3016381
ClinVar RCV Id: RCV003876532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Gly87Arg
CA9226871
NM_001173498.2:c.259G>C
CA9226872
NM_001173498.2:c.259G>A