Canonical Allele Identifier: PA2828326510
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro294Leu
CA170185
NM_001369392.2:c.881C>T