Canonical Allele Identifier: PA915958943
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66305
ClinVar RCV Id: RCV000056668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Arg388Gly
CA216829
NM_000526.5:c.1162C>G