Canonical Allele Identifier: PA658654739
Gene: KLLN HGNC NCBI

Linked Data

ClinVar Variation Id: 445578
ClinVar RCV Id: RCV000513851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119521.1:p.Phe46Cys
CA377785997
NM_001126049.2:c.137T>G