Allele Registry

Canonical Allele Identifier: PA216708

Gene: KRT5 HGNC NCBI

ClinVar RCV:

RCV000056586

RCV000249209

RCV000343050

ClinVar Variation:

66234

HGVS (amino-acid)	Matching Registered Transcripts
NP_000415.2:p.Gly138Glu	CA216707 NM_000424.4:c.413G>A