Canonical Allele Identifier: PA2829564957
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1506669
ClinVar RCV Id: RCV002006896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Leu124Val
CA415176431
NM_004992.4:c.370T>G