Canonical Allele Identifier: PA2829565130
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Val212Asp
CA415172922
NM_004992.4:c.635T>A