Canonical Allele Identifier: PA351884
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 222747
ClinVar RCV Id: RCV000208248 RCV002515548 RCV003380519
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Ile12Thr
CA351882
NM_032578.4:c.35T>C