Canonical Allele Identifier: PA105942
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9313
ClinVar RCV Id: RCV000009898 RCV000056538
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000414.2:p.Asn186Tyr
CA120294
NM_000423.3:c.556A>T