Canonical Allele Identifier: PA2827312810
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13325
ClinVar RCV Id: RCV000014253 RCV000157006 RCV000157679 RCV000587329 RCV000515213 RCV000707460 RCV002426502 RCV001813191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Ala72Gly
CA235319
NM_001330437.2:c.215C>G