Canonical Allele Identifier: PA916070115
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 640225
ClinVar RCV Id: RCV000793202

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Gln622Glu
CA376840524
NM_032578.4:c.1864C>G