Allele Registry

Canonical Allele Identifier: PA106485

Gene: KRT5 HGNC NCBI

ClinVar RCV:

RCV000015756

RCV000056615

ClinVar Variation:

14650

HGVS (amino-acid)	Matching Registered Transcripts
NP_000415.2:p.Ser181Pro	CA216749 NM_000424.4:c.541T>C