Allele Registry

Canonical Allele Identifier: PA106354

Gene: KRT5 HGNC NCBI

ClinVar RCV:

RCV000056556

ClinVar Variation:

66210

HGVS (amino-acid)	Matching Registered Transcripts
NP_000415.2:p.Ile467Thr	CA216663 NM_000424.4:c.1400T>C