Canonical Allele Identifier: PA2573168078
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 1521226
ClinVar RCV Id: RCV002046264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Pro125Arg
CA8563781
NM_000422.3:c.374C>G