Canonical Allele Identifier: PA343153
Gene: MESP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 38906
ClinVar RCV Id: RCV000032154 RCV000241739 RCV000947645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035047.1:p.Ala66Gly
CA343152
NM_001039958.2:c.197C>G