Canonical Allele Identifier: PA112243
Gene: KRT18 HGNC NCBI

Linked Data

ClinVar Variation Id: 14585
ClinVar RCV Id: RCV000015686 RCV000015687 RCV000056435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000215.1:p.His128Leu
CA124152
NM_000224.3:c.383A>T