Canonical Allele Identifier: PA101738
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 14170
ClinVar Variation Id: 208149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000521.2:p.Gly167Arg
CA123798
NM_000530.7:c.499G>C
CA347426
NM_000530.7:c.499G>A