Allele Registry

Canonical Allele Identifier: PA106298

Gene: KRT5 HGNC NCBI

ClinVar RCV:

RCV000056562

RCV001731187

ClinVar Variation:

14638

HGVS (amino-acid)	Matching Registered Transcripts
NP_000415.2:p.Glu475Gly	CA216670 NM_000424.4:c.1424A>G