Canonical Allele Identifier: PA658805433
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 503539
ClinVar RCV Id: RCV000596132 RCV002531114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Thr292Ile
CA392937406
NM_002755.4:c.875C>T