Canonical Allele Identifier: PA2828326917
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Ala88Val
CA170322
NM_001369393.2:c.263C>T