Canonical Allele Identifier: PA2827370915
Gene: PGAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50506
ClinVar RCV Id: RCV000043539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333334.1:p.Thr103Ile
CA143757
NM_001346405.1:c.308C>T