Canonical Allele Identifier: PA2826093063
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 93209
ClinVar RCV Id: RCV000079072

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Phe407Leu
CA221078
NM_001173498.2:c.1221C>A
CA404247734
NM_001173498.2:c.1221C>G
CA404247755
NM_001173498.2:c.1219T>C