Canonical Allele Identifier: PA2828328010
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Thr103Ser
CA170334
NM_001369394.2:c.308C>G
CA415173227
NM_001369394.2:c.307A>T