Canonical Allele Identifier: PA2826379114
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 960666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Val646Met
CA5522683
NM_001256267.2:c.1936G>A