Canonical Allele Identifier: PA916055539
Gene: KRT13 HGNC NCBI

Linked Data

ClinVar Variation Id: 323085
ClinVar RCV Id: RCV000274565 RCV000895674
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_705694.3:p.Arg290Gln
CA8560623
NM_153490.3:c.869G>A