Canonical Allele Identifier: PA2741991894
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2968748
ClinVar RCV Id: RCV003829394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Thr398Ser
CA403380641
NM_030662.4:c.1193C>G
CA403380646
NM_030662.4:c.1192A>T