Canonical Allele Identifier: PA2827313142
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2571898
ClinVar RCV Id: RCV003313607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Arg289Ser
CA386790485
NM_001330437.2:c.867G>C
CA386790488
NM_001330437.2:c.867G>T