Canonical Allele Identifier: PA2829069139
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Lys81Glu
CA270580
NM_001386138.1:c.241A>G