Canonical Allele Identifier: PA2828326485
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro291Leu
CA199482
NM_001369392.2:c.872C>T