Canonical Allele Identifier: PA170320
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro176Arg
CA170319
NM_004992.4:c.527C>G