Canonical Allele Identifier: PA2580127447
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2444582
ClinVar RCV Id: RCV003154366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Arg288Leu
CA399477373
NM_000526.5:c.863G>T