Canonical Allele Identifier: PA2741816398
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2760091
ClinVar RCV Id: RCV003571997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Met294Thr
CA8562584
NM_000526.5:c.881T>C