Canonical Allele Identifier: PA1139756844
Gene: KLHL40 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689606.2:p.His47Leu
CA2336578
NM_152393.3:c.140A>T