Allele Registry

Canonical Allele Identifier: PA891866075

Gene: KRT86 HGNC NCBI

ClinVar RCV:

RCV000008048

RCV000056959

ClinVar Variation:

7609

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307127.1:p.Glu413Lys	CA118924 NM_001320198.2:c.1237G>A