Canonical Allele Identifier: PA099383
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143527
ClinVar RCV Id: RCV000133059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro101Leu
CA270332
NM_004992.4:c.302C>T