Canonical Allele Identifier: PA2826955786
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Thr135Ser
CA172571
NM_001316337.2:c.404C>G
CA415172595
NM_001316337.2:c.403A>T