Canonical Allele Identifier: PA2828325996
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143590

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Thr65Ala
CA270438
NM_001369392.2:c.193A>G