Allele Registry

Canonical Allele Identifier: PA645294277

Gene: KRT16 HGNC NCBI

ClinVar RCV:

RCV000255090

ClinVar Variation:

265486

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Leu128Pro	CA10588648 NM_005557.4:c.383T>C