Canonical Allele Identifier: PA2828326078
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138187

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Thr104Met
CA199312
NM_001369392.2:c.311C>T