Canonical Allele Identifier: PA645468800
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309630
ClinVar RCV Id: RCV000405109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Gly18Arg
CA6585984
NM_000423.3:c.52G>A
CA384946129
NM_000423.3:c.52G>C