Canonical Allele Identifier: PA658805597
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 522720
ClinVar RCV Id: RCV000625873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asn320Ser
CA386791125
NM_002834.5:c.959A>G