Canonical Allele Identifier: PA2580472965
Gene: MAP2K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2140580
ClinVar RCV Id: RCV003073730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_109587.1:p.Met253Thr
CA9090835
NM_030662.4:c.758T>C