Canonical Allele Identifier: PA2499293604
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1049515
ClinVar RCV Id: RCV001355724 RCV002413840
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115967.2:p.Thr619Ile
CA376840489
NM_032578.4:c.1856C>T