Canonical Allele Identifier: PA658674961
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 477741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Asp537Tyr
CA5522627
NM_032578.4:c.1609G>T