Canonical Allele Identifier: PA2826379529
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1731203
ClinVar RCV Id: RCV003319518 RCV002452188 RCV003102372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Arg1139Cys
CA5523036
NM_001256267.2:c.3415C>T