Canonical Allele Identifier: PA916055524
Gene: KRT13 HGNC NCBI

Linked Data

ClinVar Variation Id: 323101
ClinVar RCV Id: RCV000367695 RCV001653575 RCV003972377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_705694.3:p.Ala146Gly
CA8560795
NM_153490.3:c.437C>G