Canonical Allele Identifier: PA916056601
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_542168.1:p.Asn320Ser
CA386791125
NM_080601.3:c.959A>G