Canonical Allele Identifier: PA658666665
Gene: KLHL21 HGNC NCBI

Linked Data

ClinVar Variation Id: 487795
ClinVar RCV Id: RCV000577831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055666.2:p.Glu167Asp
CA338154585
NM_014851.4:c.501G>C
CA338154587
NM_014851.4:c.501G>T