Canonical Allele Identifier: PA2828326520
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro295Leu
CA270246
NM_001369392.2:c.884C>T