Canonical Allele Identifier: PA916009353
Gene: KRT8 HGNC NCBI

Linked Data

ClinVar Variation Id: 14630
ClinVar RCV Id: RCV000015735 RCV000056938 RCV002247346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243211.1:p.Gly90Cys
CA124163
NM_001256282.2:c.268G>T