Canonical Allele Identifier: PA215340
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Leu1161Ile
CA215338
NM_032578.4:c.3481C>A