Canonical Allele Identifier: PA645426001
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 279960
ClinVar RCV Id: RCV000269273 RCV000588572 RCV000764203 RCV000824953 RCV001030088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Thr396Met
CA9090685
NM_030662.4:c.1187C>T