Canonical Allele Identifier: PA105929
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9316
ClinVar RCV Id: RCV000009901 RCV000056539
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Asn186Lys
CA120297
NM_000423.3:c.558C>A
CA384940641
NM_000423.3:c.558C>G