Canonical Allele Identifier: PA2828326712
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro387Ser
CA170251
NM_001369392.2:c.1159C>T