Canonical Allele Identifier: PA2826379097
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1305457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ser627Phe
CA376840614
NM_001256267.2:c.1880C>T