Canonical Allele Identifier: PA100849
Gene: KLHL3 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059111.2:p.Met78Val
CA269978
NM_017415.3:c.232A>G