Canonical Allele Identifier: PA2741815992
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2908434
ClinVar RCV Id: RCV003729801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Phe22Leu
CA6585980
NM_000423.3:c.64T>C
CA384945996
NM_000423.3:c.66C>G
CA384946010
NM_000423.3:c.66C>A