Canonical Allele Identifier: PA916062102
Gene: KRT18 HGNC NCBI

Linked Data

ClinVar Variation Id: 66141
ClinVar RCV Id: RCV000056442
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954657.1:p.Gln285Arg
CA216538
NM_199187.2:c.854A>G