Canonical Allele Identifier: PA199301
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro402Leu
CA199300
NM_004992.4:c.1205C>T