Allele Registry

Canonical Allele Identifier: PA107442

Gene: KRT1 HGNC NCBI

ClinVar RCV:

RCV000057082

ClinVar Variation:

66642

HGVS (amino-acid)	Matching Registered Transcripts
NP_006112.3:p.Val155Gly	CA217445 NM_006121.4:c.464T>G