Canonical Allele Identifier: PA915958902
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 66368
ClinVar RCV Id: RCV000056740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Arg148Cys
CA216961
NM_000526.5:c.442C>T