Canonical Allele Identifier: PA2826381066
Gene: KRT8 HGNC NCBI

Linked Data

ClinVar Variation Id: 66530
ClinVar RCV Id: RCV000056934 RCV003488369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243222.1:p.Lys464Asn
CA217258
NM_001256293.2:c.1392G>T
CA384992229
NM_001256293.2:c.1392G>C