Canonical Allele Identifier: PA2829564835
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1142971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.His52Gln
CA10558653
NM_004992.4:c.156C>G
CA415177813
NM_004992.4:c.156C>A