Canonical Allele Identifier: PA170341
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro199His
CA170340
NM_004992.4:c.596C>A