Canonical Allele Identifier: PA2741815935
Gene: KRT17 HGNC NCBI
ClinVar RCV:
RCV003734048
ClinVar Variation:
2902996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Leu42Pro
CA8563839
NM_000422.3:c.125T>C