Canonical Allele Identifier: PA2741991710
Gene: MAP2K2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Gln90His
CA403392460
NM_030662.4:c.270G>T
CA403392461
NM_030662.4:c.270G>C