Canonical Allele Identifier: PA2826379442
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 201888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Gln1037Arg
CA335313
NM_001256267.2:c.3110A>G