Canonical Allele Identifier: PA2826379660
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 191759
ClinVar RCV Id: RCV000172081 RCV000216203 RCV000230154 RCV000251155 RCV002470788 RCV002478552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Arg1278Gln
CA237475
NM_001256267.2:c.3833G>A