Canonical Allele Identifier: PA2827061348
Gene: COL13A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516685
ClinVar RCV Id: RCV002040902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307880.1:p.Pro385Ser
CA5534634
NM_001320951.2:c.1153C>T