Canonical Allele Identifier: PA645425855
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 254207
ClinVar RCV Id: RCV000490823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Asp71del
CA645369780
NM_030662.4:c.210_212del