Canonical Allele Identifier: PA2573096921
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1305457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Ser627Phe
CA376840614
NM_032578.4:c.1880C>T