Canonical Allele Identifier: PA2573082222
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315628
ClinVar RCV Id: RCV001755290
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ser231Leu
CA392936568
NM_002755.4:c.692C>T