Canonical Allele Identifier: PA261579
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40502
ClinVar RCV Id: RCV000033478 RCV000037639 RCV000254683 RCV000762884 RCV001813246 RCV003150934
ClinVar Variation Id: 40503
ClinVar RCV Id: RCV000037638 RCV000033479 RCV000856760 RCV000472904 RCV002453282
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu76Asp
CA261577
NM_002834.5:c.228G>C
CA261580
NM_002834.5:c.228G>T