Canonical Allele Identifier: PA2826381067
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_001243222.1:p.Gly471Glu
CA144203
NM_001256293.2:c.1412G>A