Canonical Allele Identifier: PA2828326028
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 928877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro79Thr
CA415173983
NM_001369392.2:c.235C>A