Canonical Allele Identifier: PA2828326435
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1325581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.His275Tyr
CA10558509
NM_001369392.2:c.823C>T