Canonical Allele Identifier: PA916062097
Gene: KRT18 HGNC NCBI

Linked Data

ClinVar Variation Id: 66136
ClinVar RCV Id: RCV000056437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954657.1:p.Ile150Val
CA216530
NM_199187.2:c.448A>G