Canonical Allele Identifier: PA916021419
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 411674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302420.1:p.Trp101Arg
CA16609892
NM_001315491.2:c.301T>C
CA343349532
NM_001315491.2:c.301T>A