Canonical Allele Identifier: PA645423232
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 375981
ClinVar RCV Id: RCV000426713 RCV000433235 RCV000433927 RCV000443916 RCV000444865 RCV000482718 RCV000824936 RCV000989347 RCV001250385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Pro124Ser
CA16602456
NM_002755.4:c.370C>T