Canonical Allele Identifier: PA2825181743
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2190308
ClinVar RCV Id: RCV002627999

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Val75Leu
CA9226877
NM_000528.4:c.223G>T
CA404258137
NM_000528.4:c.223G>C