Canonical Allele Identifier: PA2828326095
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95198

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Thr110Met
CA148319
NM_001369392.2:c.329C>T