Canonical Allele Identifier: PA2827312727
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181494
ClinVar RCV Id: RCV000159042 RCV001174933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn58Tyr
CA297070
NM_001330437.2:c.172A>T