Canonical Allele Identifier: PA2828326085
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1923631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro106Thr
CA10558584
NM_001369392.2:c.316C>A