Canonical Allele Identifier: PA1139745988
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 981577
ClinVar RCV Id: RCV001261097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Gln57His
CA386777529
NM_080601.3:c.171G>C
CA386777534
NM_080601.3:c.171G>T