Canonical Allele Identifier: PA645468841
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421717
ClinVar RCV Id: RCV000483744 RCV003401546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Phe189Ser
CA16619575
NM_000423.3:c.566T>C