Canonical Allele Identifier: PA170273
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143504

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro75Leu
CA170272
NM_004992.4:c.224C>T