Canonical Allele Identifier: PA099265
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly161Val
CA270449
NM_004992.4:c.482G>T