Allele Registry

Canonical Allele Identifier: PA217369

Gene: KRT6B HGNC NCBI

ClinVar RCV:

RCV000057024

RCV002496747

ClinVar Variation:

66600

HGVS (amino-acid)	Matching Registered Transcripts
NP_005546.2:p.Asn172del	CA217368 NM_005555.4:c.516_518del