Canonical Allele Identifier: PA270351
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg106Leu
CA270350
NM_004992.4:c.317G>T