Canonical Allele Identifier: PA105813
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14587
ClinVar RCV Id: RCV000015689 RCV000056512 RCV001836709 RCV002496373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Asn92Ser
CA216610
NM_000422.3:c.275A>G