Canonical Allele Identifier: PA2828326789
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro34Leu
CA270373
NM_001369393.2:c.101C>T