Canonical Allele Identifier: PA2499269706
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg91Gln
CA10558642
NM_004992.4:c.272G>A