Canonical Allele Identifier: PA270374
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro127Leu
CA270373
NM_004992.4:c.380C>T