Canonical Allele Identifier: PA2827313019
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 164998
ClinVar RCV Id: RCV000151696 RCV000380092 RCV000654965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn200Tyr
CA273218
NM_001330437.2:c.598A>T