Canonical Allele Identifier: PA2829564928
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 521464
ClinVar RCV Id: RCV000624621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Trp104Cys
CA415176854
NM_004992.4:c.312G>T
CA415176857
NM_004992.4:c.312G>C