Canonical Allele Identifier: PA2829068588
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro99Ala
CA274540
NM_001386137.1:c.295C>G