Canonical Allele Identifier: PA2826379465
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2299618
ClinVar RCV Id: RCV004153925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Val1058Ala
CA376858122
NM_001256267.2:c.3173T>C