Canonical Allele Identifier: PA658664269
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 477666
ClinVar RCV Id: RCV000547883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asp43del
CA658656490
NM_002755.4:c.129_131del