Canonical Allele Identifier: PA101222
Gene: KLHL10 HGNC NCBI

Linked Data

ClinVar Variation Id: 40008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689680.2:p.Gln216Pro
CA130709
NM_152467.5:c.647A>C