Canonical Allele Identifier: PA2826379080
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 31829
ClinVar RCV Id: RCV000024522 RCV004018674
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Glu614Lys
CA215365
NM_001256267.2:c.1840G>A