Canonical Allele Identifier: PA2827312723
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 981577
ClinVar RCV Id: RCV001261097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Gln57His
CA386777529
NM_001330437.2:c.171G>C
CA386777534
NM_001330437.2:c.171G>T