Canonical Allele Identifier: PA170404
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ile303Met
CA170403
NM_004992.4:c.909C>G