ClinGen Allele Registry
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Canonical Allele Identifier:
PA916056891
Gene: MAP2K2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000824698
RCV003313157
RCV003908112
ClinVar Variation:
666272
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_109587.1:p.Pro128Leu
CA9091012
NM_030662.4:c.383C>T