Canonical Allele Identifier: PA106872
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13352
ClinVar Variation Id: 40745
ClinVar RCV Id: RCV000158013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Gly128Val
CA280038
NM_002755.4:c.383G>T
CA296125
NM_002755.4:c.383_384delinsTT