Canonical Allele Identifier: PA1139669880
Gene: HOXD13 HGNC NCBI

Linked Data

ClinVar Variation Id: 930707
ClinVar RCV Id: RCV001196568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000514.2:p.Gly237Arg
CA349353320
NM_000523.4:c.709G>A
CA349353321
NM_000523.4:c.709G>C