Allele Registry

Canonical Allele Identifier: PA134624

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV000037602

RCV000519375

RCV001719721

RCV004018723

RCV004532502

ClinVar Variation:

40756

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Ala283Val	CA134622 NM_002755.4:c.848C>T