Canonical Allele Identifier: PA2741991827
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2832213
ClinVar RCV Id: RCV003655843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Pro296Ser
CA403385251
NM_030662.4:c.886C>T