Canonical Allele Identifier: PA170270
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro72Leu
CA170269
NM_004992.4:c.215C>T