Allele Registry

Canonical Allele Identifier: PA106538

Gene: KRT5 HGNC NCBI

ClinVar RCV:

RCV000056625

RCV001352726

RCV001731298

ClinVar Variation:

14652

HGVS (amino-acid)	Matching Registered Transcripts
NP_000415.2:p.Val186Leu	CA216764 NM_000424.4:c.556G>T CA384928636 NM_000424.4:c.556G>C