Canonical Allele Identifier: PA134627
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 44593
ClinVar RCV Id: RCV000037603 RCV001852782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Thr292Ser
CA134625
NM_002755.4:c.875C>G
CA392937404
NM_002755.4:c.874A>T