Canonical Allele Identifier: PA2826093142
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208267
ClinVar RCV Id: RCV000206955
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Ser452Tyr
CA350955
NM_001173498.2:c.1355C>A