Canonical Allele Identifier: PA2826379935
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1049515
ClinVar RCV Id: RCV001355724 RCV002413840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Thr325Ile
CA376840489
NM_001256268.2:c.974C>T