Canonical Allele Identifier: PA297078
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181496
ClinVar RCV Id: RCV000159045 RCV001813410 RCV002288669 RCV002281971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Glu76Gln
CA297076
NM_002834.5:c.226G>C