Canonical Allele Identifier: PA915958823
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 781859
ClinVar RCV Id: RCV000963160 RCV002489369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Arg56Cys
CA8562802
NM_000526.5:c.166C>T