Canonical Allele Identifier: PA280065
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Asn126Ser
CA280064
NM_004992.4:c.377A>G