Canonical Allele Identifier: PA645423268
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372605
ClinVar RCV Id: RCV000413673 RCV000654948 RCV003298420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Arg291Gly
CA7624026
NM_002755.4:c.871A>G