Canonical Allele Identifier: PA2826918383
Gene: MAP4K2 HGNC NCBI

Linked Data

ClinVar Variation Id: 776623
ClinVar RCV Id: RCV000956958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001294919.1:p.Arg572His
CA6081387
NM_001307990.2:c.1715G>A