Canonical Allele Identifier: PA2829069132
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro79Ala
CA270565
NM_001386138.1:c.235C>G