Canonical Allele Identifier: PA2828325268
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Thr135Ser
CA172571
NM_001369391.2:c.404C>G
CA415172595
NM_001369391.2:c.403A>T