Allele Registry

Canonical Allele Identifier: PA200040

Gene: MYPN HGNC NCBI

ClinVar Allele:

40460

ClinVar RCV:

RCV000024493

RCV000172772

RCV000252665

RCV000625362

RCV001778667

ClinVar Variation:

31800

HGVS (amino-acid)	Matching Registered Transcripts
NP_115967.2:p.Pro1135Thr	CA200038 NM_032578.4:c.3403C>A