Canonical Allele Identifier: PA2826379434
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1351599
ClinVar RCV Id: RCV002044848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ser1031Pro
CA376857335
NM_001256267.2:c.3091T>C