Canonical Allele Identifier: PA916009377
Gene: KRT8 HGNC NCBI

Linked Data

ClinVar Variation Id: 56170
ClinVar RCV Id: RCV000049581 RCV004018966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243211.1:p.Gly499Glu
CA144203
NM_001256282.2:c.1496G>A