Canonical Allele Identifier: PA2829565264
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 386725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ala281Thr
CA10558543
NM_004992.4:c.841G>A