Canonical Allele Identifier: PA2827313195
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 522720
ClinVar RCV Id: RCV000625873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asn320Ser
CA386791125
NM_001330437.2:c.959A>G