Canonical Allele Identifier: PA217246
Gene: KRT8 HGNC NCBI

Linked Data

ClinVar Variation Id: 66522
ClinVar RCV Id: RCV000056926
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002264.1:p.Arg341His
CA217245
NM_002273.4:c.1022G>A