Canonical Allele Identifier: PA112233
Gene: KRT18 HGNC NCBI

Linked Data

ClinVar Variation Id: 66131
ClinVar RCV Id: RCV000056431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000215.1:p.Gly340Arg
CA216523
NM_000224.3:c.1018G>A
CA385007206
NM_000224.3:c.1018G>C