Allele Registry

Canonical Allele Identifier: PA1139700544

Gene: MAP2K1 HGNC NCBI

ClinVar RCV:

RCV001261060

ClinVar Variation:

981553

HGVS (amino-acid)	Matching Registered Transcripts
NP_002746.1:p.Ile103Thr	CA392930305 NM_002755.4:c.308T>C