Allele Registry

Canonical Allele Identifier: PA101567

Gene: MPZ HGNC NCBI

ClinVar RCV:

RCV000790098

RCV000813380

ClinVar Variation:

242747

HGVS (amino-acid)	Matching Registered Transcripts
NP_000521.2:p.Asp128Asn	CA351448 NM_000530.7:c.382G>A