Canonical Allele Identifier: PA2741991873
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3021502
ClinVar RCV Id: RCV003875125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Thr364Ala
CA403382420
NM_030662.4:c.1090A>G