Allele Registry

Canonical Allele Identifier: PA220145

Gene: PTPN11 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

49037

799666

ClinVar RCV:

RCV000077854

RCV000521890

RCV001001798

RCV001171895

RCV001261024

RCV002399355

RCV002490449

RCV003147312

RCV003147313

RCV003147314

RCV003989616

RCV004528333

RCV004532497

ClinVar Variation:

40567

811634

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_002825.3:p.Gln510His	CA220143 NM_002834.5:c.1530G>C CA386779921 NM_002834.5:c.1530G>T