Allele Registry

Canonical Allele Identifier: PA916009733

Gene: MIPEP HGNC NCBI

ClinVar RCV:

RCV000412643

RCV000616145

ClinVar Variation:

208629

HGVS (amino-acid)	Matching Registered Transcripts
NP_005923.3:p.Leu71Gln	CA16040609 NM_005932.4:c.212T>A