Canonical Allele Identifier: PA915975014
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_004570.2:p.Arg580His
CA6081387
NM_004579.5:c.1739G>A