Canonical Allele Identifier: PA2826379892
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1955577
ClinVar RCV Id: RCV002695495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Pro280Ala
CA376839898
NM_001256268.2:c.838C>G