This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2741894697
Gene: MAP2K1 HGNC NCBI
ClinVar RCV:
RCV003228318
ClinVar Variation:
2501899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ile361_Lys362delinsGlu
CA2580613854
NM_002755.4:c.1081_1084delinsG