Canonical Allele Identifier: PA204852
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 208765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000521.2:p.Cys127Ser
CA204850
NM_000530.7:c.380G>C
CA343348890
NM_000530.7:c.379T>A