Canonical Allele Identifier: PA186108
Gene: PTRH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 183332
ClinVar RCV Id: RCV000162156 RCV000162247 RCV001799627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001015509.1:p.Gln86Pro
CA186106
NM_001015509.3:c.257A>C