Canonical Allele Identifier: PA916028148
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40553
ClinVar RCV Id: RCV000033539 RCV000055885 RCV000254686 RCV000722171 RCV000824747 RCV001813259 RCV002490447 RCV004018715 RCV004532493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Arg502Trp
CA273451
NM_001330437.2:c.1504C>T