Canonical Allele Identifier: PA916009357
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_001243211.1:p.Arg369His
CA217245
NM_001256282.2:c.1106G>A