Canonical Allele Identifier: PA279998
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40744
ClinVar RCV Id: RCV000037595 RCV000424633 RCV000436322 RCV000435315 RCV000417448 RCV000425638 RCV000680623 RCV001542689 RCV001813306 RCV002513329
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Pro124Leu
CA279996
NM_002755.4:c.371C>T