Canonical Allele Identifier: PA645451840
Gene: MESP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 317385
ClinVar RCV Id: RCV000348753 RCV000909848 RCV002522810 RCV003920337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035047.1:p.Arg62Gln
CA7730362
NM_001039958.2:c.185G>A