Allele Registry

Canonical Allele Identifier: PA916009764

Gene: MIPEP HGNC NCBI

ClinVar RCV:

RCV000412562

RCV000610224

ClinVar Variation:

208628

HGVS (amino-acid)	Matching Registered Transcripts
NP_005923.3:p.Leu582Arg	CA16040608 NM_005932.4:c.1745T>G