ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA180892
Gene: MAP2K2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
177868
ClinVar RCV Id:
RCV000154507
RCV000208747
RCV000412815
RCV000844676
RCV003453160
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_109587.1:p.Tyr134Cys
CA180890
NM_030662.4:c.401A>G