Canonical Allele Identifier: PA216617
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 66185
ClinVar RCV Id: RCV000056519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Ala96_Leu99del
CA216616
NM_000422.3:c.287_298del