Allele Registry

Canonical Allele Identifier: PA229199

Gene: KRT82 HGNC NCBI

ClinVar Allele:

106745

ClinVar RCV:

RCV000087247

ClinVar Variation:

100885

HGVS (amino-acid)	Matching Registered Transcripts
NP_149022.3:p.Glu210Asp	CA229198 NM_033033.4:c.630G>C CA384939108 NM_033033.4:c.630G>T