Canonical Allele Identifier: PA916028153
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40556
ClinVar RCV Id: RCV000033542 RCV000212898 RCV001731329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Ser506Ala
CA273454
NM_001330437.2:c.1516T>G