ClinGen Allele Registry
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Canonical Allele Identifier:
PA280076
Gene: MAP2K2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000158039
RCV000200295
RCV001205317
RCV001781338
ClinVar Variation:
40769
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_109587.1:p.Lys61Glu
CA280074
NM_030662.4:c.181A>G