Canonical Allele Identifier: PA916056565
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40525
ClinVar RCV Id: RCV000033505 RCV000077860 RCV000824745 RCV001283770 RCV001731328 RCV001813250 RCV002054539 RCV002273940 RCV002444453 RCV003153317 RCV003387505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Ile282Val
CA220152
NM_080601.3:c.844A>G