Canonical Allele Identifier: PA2827313218
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 1188270
ClinVar RCV Id: RCV001547997 RCV003655335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Met344Ile
CA386791503
NM_001330437.2:c.1032G>A
CA386791504
NM_001330437.2:c.1032G>C
CA386791506
NM_001330437.2:c.1032G>T