Allele Registry

Canonical Allele Identifier: PA217376

Gene: KRT16 HGNC NCBI

ClinVar RCV:

RCV000057029

ClinVar Variation:

66604

HGVS (amino-acid)	Matching Registered Transcripts
NP_005548.2:p.Met121Lys	CA217375 NM_005557.4:c.362T>A