Canonical Allele Identifier: PA2573078701
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143659
ClinVar RCV Id: RCV000133200 RCV000460836 RCV001719908 RCV003990996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Ser6Leu
CA170358
NM_001386139.1:c.17C>T