ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828530602
Gene: PTPN11
HGNC
NCBI
Linked Data
ClinVar Variation Id:
181499
ClinVar RCV Id:
RCV000159051
RCV001261017
RCV001526955
RCV002408715
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001361554.1:p.Phe284Tyr
CA297085
NM_001374625.1:c.851T>A