Canonical Allele Identifier: PA2828326696
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2848886
ClinVar RCV Id: RCV003640217
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Pro376Leu
CA415163451
NM_001369392.2:c.1127C>T