Canonical Allele Identifier: PA170317
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro173Arg
CA170316
NM_004992.4:c.518C>G