Canonical Allele Identifier: PA2829565124
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 928876
ClinVar RCV Id: RCV001193433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Val209Leu
CA415172963
NM_004992.4:c.625G>T
CA415172966
NM_004992.4:c.625G>C