Canonical Allele Identifier: PA2829565053
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 928877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro172Thr
CA415173983
NM_004992.4:c.514C>A