Canonical Allele Identifier: PA2826093929
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2995667
ClinVar RCV Id: RCV003853754
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Met911Ile
CA404237965
NM_001173498.2:c.2733G>T
CA404237967
NM_001173498.2:c.2733G>C
CA404237969
NM_001173498.2:c.2733G>A