Canonical Allele Identifier: PA2826093237
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2145938
ClinVar RCV Id: RCV003066874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Arg508Cys
CA9226422
NM_001173498.2:c.1522C>T