Canonical Allele Identifier: PA2826379096
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 520317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ser627Thr
CA376840605
NM_001256267.2:c.1879T>A