Canonical Allele Identifier: PA915993230
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 597127
ClinVar RCV Id: RCV000733155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Val119Leu
CA404256576
NM_001173498.2:c.355G>T
CA404256577
NM_001173498.2:c.355G>C