Canonical Allele Identifier: PA915958975
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Tyr415Cys
CA216863
NM_000526.5:c.1244A>G