Canonical Allele Identifier: PA2573224447
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1677929
ClinVar RCV Id: RCV002224520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Arg227Ser
CA392936523
NM_002755.4:c.681G>T
CA392936525
NM_002755.4:c.681G>C