Canonical Allele Identifier: PA2573224351
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440001
ClinVar RCV Id: RCV001978742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Gly80Ser
CA392929437
NM_002755.4:c.238G>A