Canonical Allele Identifier: PA296108
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40780
ClinVar RCV Id: RCV000158003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Val60Gly
CA296106
NM_002755.4:c.179T>G