Canonical Allele Identifier: PA1139761740
Gene: PIGW HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848612.2:p.Thr200Ile
CA290116071
NM_178517.5:c.599C>T