Canonical Allele Identifier: PA2825181744
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 657499
ClinVar RCV Id: RCV000814108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Val75Glu
CA305479006
NM_000528.4:c.224T>A