Canonical Allele Identifier: PA174538
Gene: PTPN21 HGNC NCBI

Linked Data

ClinVar Variation Id: 161654
ClinVar RCV Id: RCV000149190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008970.2:p.Asn32His
CA174537
NM_007039.4:c.94A>C