Canonical Allele Identifier: PA916028137
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13343
ClinVar RCV Id: RCV000033531 RCV000055883 RCV000077850 RCV000824746 RCV001281363 RCV001813203 RCV002390105 RCV004532346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gly468Ala
CA220131
NM_001330437.2:c.1403G>C