Canonical Allele Identifier: PA2829372239
Gene: KRT13 HGNC NCBI

Linked Data

ClinVar Variation Id: 323105
ClinVar RCV Id: RCV000268820
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002265.3:p.Asp113Asn
CA10645621
NM_002274.4:c.337G>A