Canonical Allele Identifier: PA2829070004
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Arg255Gln
CA199452
NM_001386139.1:c.764G>A