Canonical Allele Identifier: PA180745
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40781
ClinVar RCV Id: RCV000158004 RCV000192193 RCV000208771 RCV000212506 RCV000423708 RCV000439184 RCV000754677 RCV000844673 RCV001095724 RCV002415455 RCV003224114
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Asp67Asn
CA180743
NM_002755.4:c.199G>A