Canonical Allele Identifier: PA2829565004
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 717385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr148Ala
CA415174791
NM_004992.4:c.442A>G