Canonical Allele Identifier: PA2580473069
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1710619
ClinVar RCV Id: RCV002291906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Thr398Pro
CA403380651
NM_030662.4:c.1192A>C