Canonical Allele Identifier: PA915969972
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 666420
ClinVar RCV Id: RCV000824937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Pro193Ala
CA392936079
NM_002755.4:c.577C>G