Canonical Allele Identifier: PA916062110
Gene: KRT18 HGNC NCBI

Linked Data

ClinVar Variation Id: 66131
ClinVar RCV Id: RCV000056431
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_954657.1:p.Gly340Arg
CA216523
NM_199187.2:c.1018G>A
CA385007206
NM_199187.2:c.1018G>C