Canonical Allele Identifier: PA2826379090
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 640225
ClinVar RCV Id: RCV000793202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Gln622Glu
CA376840524
NM_001256267.2:c.1864C>G