Canonical Allele Identifier: PA891866065
Gene: KRT86 HGNC NCBI

Linked Data

ClinVar Variation Id: 66547
ClinVar RCV Id: RCV000056961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307127.1:p.Arg66His
CA217290
NM_001320198.2:c.197G>A