Canonical Allele Identifier: PA2826379959
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1782397
ClinVar RCV Id: RCV002408352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243197.1:p.Ala342Thr
CA208192990
NM_001256268.2:c.1024G>A