Canonical Allele Identifier: PA2580158055
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2190308
ClinVar RCV Id: RCV002627999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Val75Leu
CA9226877
NM_001173498.2:c.223G>T
CA404258137
NM_001173498.2:c.223G>C