Canonical Allele Identifier: PA913201676
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40554
ClinVar RCV Id: RCV000033540 RCV000055886 RCV000212896 RCV000626828 RCV000494687 RCV000824748 RCV001813260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Arg502Leu
CA273434
NM_001330437.2:c.1505G>T