Canonical Allele Identifier: PA658829297
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 561346
ClinVar RCV Id: RCV000680631 RCV001204172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Pro265Ser
CA392937202
NM_002755.4:c.793C>T