Canonical Allele Identifier: PA2828530379
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2756656
ClinVar RCV Id: RCV003540328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Tyr61Ser
CA386777608
NM_001374625.1:c.182A>C