Canonical Allele Identifier: PA2829565057
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 804125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro173Thr
CA415173958
NM_004992.4:c.517C>A