Canonical Allele Identifier: PA2580112193
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2377370
ClinVar RCV Id: RCV002670490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Gly25Ser
CA6585976
NM_000423.3:c.73G>A