Canonical Allele Identifier: PA104162
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Gln122Pro
CA217378
NM_005557.4:c.365A>C