Canonical Allele Identifier: PA658818334
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 520319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Gly634Arg
CA5522679
NM_032578.4:c.1900G>A
CA376840711
NM_032578.4:c.1900G>C