Allele Registry

Canonical Allele Identifier: PA916009756

Gene: MIPEP HGNC NCBI

ClinVar RCV:

RCV000412622

RCV000616524

ClinVar Variation:

208632

HGVS (amino-acid)	Matching Registered Transcripts
NP_005923.3:p.Lys343Glu	CA16040611 NM_005932.4:c.1027A>G