Canonical Allele Identifier: PA645423251
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375982
ClinVar RCV Id: RCV000418114 RCV001266169 RCV003329162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Glu203Lys
CA16602457
NM_002755.4:c.607G>A