Canonical Allele Identifier: PA916059429
Gene: PKHD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733842.2:p.Val1741Met
CA234572
NM_170724.3:c.5221G>A