Canonical Allele Identifier: PA658805396
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 503541
ClinVar RCV Id: RCV000593777 RCV000681073 RCV001860225 RCV001813514
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Lys84Arg
CA7623881
NM_002755.4:c.251A>G