Canonical Allele Identifier: PA216539
Gene: KRT18 HGNC NCBI

Linked Data

ClinVar Variation Id: 66141
ClinVar RCV Id: RCV000056442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000215.1:p.Gln285Arg
CA216538
NM_000224.3:c.854A>G