Canonical Allele Identifier: PA2829565072
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro179Ala
CA415173835
NM_004992.4:c.535C>G