Canonical Allele Identifier: PA2580112131
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 1945945
ClinVar RCV Id: RCV002667441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Gly68Asp
CA8563819
NM_000422.3:c.203G>A