Canonical Allele Identifier: PA2830086770
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1026688
ClinVar RCV Id: RCV001327168 RCV004035232
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.His1129Arg
CA5523033
NM_032578.4:c.3386A>G