Canonical Allele Identifier: PA2829599004
Gene: KRT16 HGNC NCBI

Linked Data

ClinVar Variation Id: 3116339
ClinVar RCV Id: RCV004412203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005548.2:p.Ser17Thr
CA399497151
NM_005557.4:c.49T>A