Canonical Allele Identifier: PA2827312805
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 41443
ClinVar RCV Id: RCV000420663 RCV000413699 RCV000425022 RCV000431335 RCV000434875 RCV003654183
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Ala72Val
CA215451
NM_001330437.2:c.215C>T
CA645580458
NM_001330437.2:c.215_216delinsTT