Canonical Allele Identifier: PA2828325047
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Val29Met
CA270366
NM_001369391.2:c.85G>A