Canonical Allele Identifier: PA2829379048
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3222783
ClinVar RCV Id: RCV004516167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Arg295Gly
CA392937418
NM_002755.4:c.883A>G