Allele Registry

Canonical Allele Identifier: PA2829859961

Gene: MAN1B1 HGNC NCBI

ClinVar RCV:

RCV003081561

ClinVar Variation:

2153987

HGVS (amino-acid)	Matching Registered Transcripts
NP_057303.2:p.Ala683Thr	CA375709242 NM_016219.5:c.2047G>A CA2580080959 NM_016219.5:c.2046_2047delinsCA