Canonical Allele Identifier: PA645383793
Gene: MAB21L2 HGNC NCBI

Linked Data

ClinVar Variation Id: 427785
ClinVar RCV Id: RCV000490802
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006430.1:p.Arg51Gly
CA358602408
NM_006439.5:c.151C>G