Canonical Allele Identifier: PA645468825
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 309618
ClinVar RCV Id: RCV000370371 RCV000434387
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Arg179His
CA6585819
NM_000423.3:c.536G>A