Canonical Allele Identifier: PA106062
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9312
ClinVar RCV Id: RCV000009897 RCV000056529
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Thr479Pro
CA120293
NM_000423.3:c.1435A>C