Canonical Allele Identifier: PA2580263488
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1903178
ClinVar RCV Id: RCV002583494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Arg295Ser
CA392937423
NM_002755.4:c.885G>C
CA392937424
NM_002755.4:c.885G>T