Canonical Allele Identifier: PA2829565179
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ala239Asp
CA415172315
NM_004992.4:c.716C>A