Canonical Allele Identifier: PA1139687359
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 942308
ClinVar RCV Id: RCV001212270 RCV001587228 RCV002322031 RCV002497724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Thr752Pro
CA5522956
NM_001256268.2:c.2254A>C