Canonical Allele Identifier: PA2580112136
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 2361893
ClinVar RCV Id: RCV002980651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Ser71Arg
CA8563818
NM_000422.3:c.213C>A
CA399512900
NM_000422.3:c.213C>G
CA399512912
NM_000422.3:c.211A>C