Canonical Allele Identifier: PA915958980
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 14623
ClinVar RCV Id: RCV000056692 RCV001731186
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Glu422Lys
CA216874
NM_000526.5:c.1264G>A