Canonical Allele Identifier: PA2741991897
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2548628
ClinVar RCV Id: RCV004321635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Val400Leu
CA403380610
NM_030662.4:c.1198G>T
CA403380613
NM_030662.4:c.1198G>C