Canonical Allele Identifier: PA109547
Gene: MAB21L2 HGNC NCBI

Linked Data

ClinVar Variation Id: 139620
ClinVar RCV Id: RCV000128563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006430.1:p.Arg51His
CA163332
NM_006439.5:c.152G>A