Canonical Allele Identifier: PA2826093552
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208284
ClinVar RCV Id: RCV000206950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Trp713Arg
CA350952
NM_001173498.2:c.2137T>C
CA404243199
NM_001173498.2:c.2137T>A