Canonical Allele Identifier: PA2826380361
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 969327

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Met1011Ile
CA376830326
NM_001256268.2:c.3033G>A
CA376830327
NM_001256268.2:c.3033G>C
CA376830328
NM_001256268.2:c.3033G>T