Canonical Allele Identifier: PA2827313195
Gene: PTPN11 HGNC NCBI
ClinVar RCV:
RCV000625873
ClinVar Variation:
522720
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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