Canonical Allele Identifier: PA101577
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 637785
ClinVar RCV Id: RCV000790101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000521.2:p.Asp128Glu
CA343348839
NM_000530.7:c.384C>G
CA343348843
NM_000530.7:c.384C>A