ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA137934
Gene: MAP2K2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000039479
RCV003764692
ClinVar Variation:
46234
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_109587.1:p.Val131Met
CA137932
NM_030662.4:c.391G>A