Canonical Allele Identifier: PA2825182058
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2433630
ClinVar RCV Id: RCV003132586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Gly255Arg
CA404252500
NM_000528.4:c.763G>C