Allele Registry

Canonical Allele Identifier: PA645294276

Gene: KRT16 HGNC NCBI

ClinVar Allele:

260165

ClinVar RCV:

RCV000255715

RCV002494798

ClinVar Variation:

265217

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Arg127Gly	CA10588649 NM_005557.4:c.379C>G