Canonical Allele Identifier: PA2826379085
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1049515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Thr619Ile
CA376840489
NM_001256267.2:c.1856C>T