Canonical Allele Identifier: PA270247
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro388Leu
CA270246
NM_004992.4:c.1163C>T