Canonical Allele Identifier: PA2830086607
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_115967.2:p.Thr1046Pro
CA5522956
NM_032578.4:c.3136A>C