Canonical Allele Identifier: PA104244
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 14608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Met121Thr
CA217377
NM_005557.4:c.362T>C