Canonical Allele Identifier: PA2829372266
Gene: KRT13 HGNC NCBI

Linked Data

ClinVar Variation Id: 323095
ClinVar RCV Id: RCV000342351
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002265.3:p.Val204Met
CA8560707
NM_002274.4:c.610G>A