Canonical Allele Identifier: PA105980
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9314
ClinVar RCV Id: RCV000009899 RCV000056527
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Glu476Lys
CA120295
NM_000423.3:c.1426G>A