Allele Registry

Canonical Allele Identifier: PA891866067

Gene: KRT86 HGNC NCBI

ClinVar RCV:

RCV000008051

RCV000056963

ClinVar Variation:

7612

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307127.1:p.Asn114Asp	CA118927 NM_001320198.2:c.340A>G