Canonical Allele Identifier: PA2829565150
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3016198
ClinVar RCV Id: RCV003876349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gln227His
CA10558567
NM_004992.4:c.681A>C
CA10558569
NM_004992.4:c.681A>T