Canonical Allele Identifier: PA2829565120
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 290402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Val207Ala
CA10606762
NM_004992.4:c.620T>C