Canonical Allele Identifier: PA170314
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro172Leu
CA170313
NM_004992.4:c.515C>T