Canonical Allele Identifier: PA2826379035
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 640837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Glu566Gln
CA376839794
NM_001256267.2:c.1696G>C