Canonical Allele Identifier: PA916028134
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13342
ClinVar RCV Id: RCV000033530 RCV000037611 RCV000055882 RCV000529342 RCV001002017 RCV001089941 RCV004532345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Ala465Thr
CA261534
NM_001330437.2:c.1393G>A