Allele Registry

Canonical Allele Identifier: PA2830086796

Gene: MYPN HGNC NCBI

ClinVar Variation Id: 1731203

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Arg1139Cys	CA5523036 NM_032578.4:c.3415C>T