Allele Registry

Canonical Allele Identifier: PA106366

Gene: KRT5 HGNC NCBI

ClinVar RCV:

RCV000056608

RCV001731188

ClinVar Variation:

14645

HGVS (amino-acid)	Matching Registered Transcripts
NP_000415.2:p.Leu175Phe	CA216739 NM_000424.4:c.523C>T