Canonical Allele Identifier: PA2826381051
Gene: KRT8 HGNC NCBI

Linked Data

ClinVar Variation Id: 66522
ClinVar RCV Id: RCV000056926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243222.1:p.Arg341His
CA217245
NM_001256293.2:c.1022G>A