Canonical Allele Identifier: PA2580263439
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1719165
ClinVar RCV Id: RCV002301925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ser86Thr
CA392929514
NM_002755.4:c.256T>A