Canonical Allele Identifier: PA104206
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Leu128Gln
CA217386
NM_005557.4:c.383T>A