Canonical Allele Identifier: PA2826379498
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1729911
ClinVar RCV Id: RCV002326190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Pro1100Leu
CA376858901
NM_001256267.2:c.3299C>T