Canonical Allele Identifier: PA119582
Gene: GDF5 HGNC NCBI

Linked Data

ClinVar Variation Id: 8394
ClinVar RCV Id: RCV000008902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000548.2:p.Pro436Thr
CA119581
NM_000557.5:c.1306C>A