This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2741927631
Gene: HOXC9 HGNC NCBI
ClinVar RCV:
RCV004324558
ClinVar Variation:
2553763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008828.1:p.Arg234Trp
CA385116685
NM_006897.3:c.700C>T