Allele Registry

Canonical Allele Identifier: PA109541

Gene: MAB21L2 HGNC NCBI

ClinVar RCV:

RCV000128564

ClinVar Variation:

139621

HGVS (amino-acid)	Matching Registered Transcripts
NP_006430.1:p.Arg51Cys	CA163333 NM_006439.5:c.151C>T