Canonical Allele Identifier: PA2573168077
Gene: KRT17 HGNC NCBI
ClinVar RCV:
RCV001924658
ClinVar Variation:
1383730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Pro125Thr
CA8563783
NM_000422.3:c.373C>A