Canonical Allele Identifier: PA1139700607
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 981554
ClinVar RCV Id: RCV001261061 RCV001349797
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Glu203Ala
CA392936203
NM_002755.4:c.608A>C