Canonical Allele Identifier: PA916056601
Gene: PTPN11 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asn320Ser
CA386791125
NM_080601.3:c.959A>G