Canonical Allele Identifier: PA2573078749
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Ile80Met
CA170403
NM_001386139.1:c.240C>G