Canonical Allele Identifier: PA2826379109
Gene: MYPN HGNC NCBI

Linked Data

ClinVar Variation Id: 1782397
ClinVar RCV Id: RCV002408352

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243196.1:p.Ala636Thr
CA208192990
NM_001256267.2:c.1906G>A