Canonical Allele Identifier: PA102038
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 411669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000521.2:p.Ser78Trp
CA16609896
NM_000530.7:c.233C>G