ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA170314
Gene: MECP2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
143607
ClinVar RCV Id:
RCV000133147
RCV002055854
RCV002336286
RCV003990988
RCV004532603
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004983.1:p.Pro172Leu
CA170313
NM_004992.4:c.515C>T