Canonical Allele Identifier: PA2825559268
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1745655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro184Ala
CA415173980
NM_001110792.2:c.550C>G