ClinGen Allele Registry
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Canonical Allele Identifier:
PA2827313123
Gene: PTPN11
HGNC
NCBI
Linked Data
ClinVar Variation Id:
13335
ClinVar RCV Id:
RCV000014263
RCV000037663
RCV000077862
RCV000190417
RCV000458650
RCV001376066
RCV001813200
RCV004532343
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001317366.1:p.Phe285Ser
CA204408
NM_001330437.2:c.854T>C