Canonical Allele Identifier: PA101677
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 14195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000521.2:p.Glu97Val
CA257172
NM_000530.7:c.290A>T