Canonical Allele Identifier: PA2826379121
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 2049015
ClinVar RCV Id: RCV002932176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Pro651Thr
CA376841051
NM_001256267.2:c.1951C>A