Canonical Allele Identifier: PA2829565081
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2117601
ClinVar RCV Id: RCV003027825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly185Cys
CA415173667
NM_004992.4:c.553G>T