Canonical Allele Identifier: PA2573171033
Gene: KRT14 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436350
ClinVar RCV Id: RCV001987327
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000517.3:p.Asp142Asn
CA8562722
NM_000526.5:c.424G>A