Canonical Allele Identifier: PA2741991885
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2898766
ClinVar RCV Id: RCV003654694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Thr386Asn
CA403380865
NM_030662.4:c.1157C>A