Canonical Allele Identifier: PA2828530356
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 981577
ClinVar RCV Id: RCV001261097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Gln56His
CA386777529
NM_001374625.1:c.168G>C
CA386777534
NM_001374625.1:c.168G>T