Canonical Allele Identifier: PA2826381059
Gene: KRT8 HGNC NCBI

Linked Data

ClinVar Variation Id: 66528
ClinVar RCV Id: RCV000056932 RCV003935000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243222.1:p.Gly434Ser
CA217254
NM_001256293.2:c.1300G>A