Canonical Allele Identifier: PA2829565100
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1604076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro199Ser
CA415173156
NM_004992.4:c.595C>T