Allele Registry

Canonical Allele Identifier: PA2827312749

Gene: PTPN11 HGNC NCBI

ClinVar Allele:

70453

ClinVar RCV:

RCV000049228

RCV000414941

RCV001813372

RCV002287357

RCV002513672

RCV003224860

ClinVar Variation:

55797

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317366.1:p.Gly60Val	CA284662 NM_001330437.2:c.179G>T