Canonical Allele Identifier: PA274840
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 192293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro217Ser
CA274839
NM_004992.4:c.649C>T