Canonical Allele Identifier: PA2829565080
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1166038
ClinVar RCV Id: RCV001513735 RCV001724326
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr184Ser
CA10558593
NM_004992.4:c.551C>G
CA415173706
NM_004992.4:c.550A>T