Canonical Allele Identifier: PA916055530
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_705694.3:p.Val204Met
CA8560707
NM_153490.3:c.610G>A