Canonical Allele Identifier: PA294705
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156665
ClinVar RCV Id: RCV000144808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly185Ser
CA294704
NM_004992.4:c.553G>A