Canonical Allele Identifier: PA2826379105
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 379702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Arg631Lys
CA16606036
NM_001256267.2:c.1892G>A