Canonical Allele Identifier: PA270459
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro173Ala
CA270458
NM_004992.4:c.517C>G