Canonical Allele Identifier: PA2741816427
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2515383
ClinVar RCV Id: RCV003252115

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Ala479Val
CA9226439
NM_000528.4:c.1436C>T