Canonical Allele Identifier: PA099211
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Asp156Gly
CA270431
NM_004992.4:c.467A>G