Canonical Allele Identifier: PA2826956176
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro295Leu
CA270246
NM_001316337.2:c.884C>T