Canonical Allele Identifier: PA2829565077
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro182Ser
CA415173760
NM_004992.4:c.544C>T