Canonical Allele Identifier: PA2826093185
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93210
ClinVar RCV Id: RCV000079073 RCV000295977 RCV000675480
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Ala480Ser
CA146745
NM_001173498.2:c.1438G>T