Canonical Allele Identifier: PA2741816273
Gene: HOXA13 HGNC NCBI

Linked Data

ClinVar Variation Id: 3047699
ClinVar RCV Id: RCV003949625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000513.2:p.Asn189Ser
CA155875417
NM_000522.5:c.566A>G