Canonical Allele Identifier: PA915993218
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 657499
ClinVar RCV Id: RCV000814108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Val75Glu
CA305479006
NM_001173498.2:c.224T>A