Canonical Allele Identifier: PA2741815945
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 2579370
ClinVar RCV Id: RCV003327805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Ala81Val
CA8563808
NM_000422.3:c.242C>T
CA2580617964
NM_000422.3:c.242_243delinsTC