Canonical Allele Identifier: PA2580341493
Gene: HOXB13 HGNC NCBI
ClinVar RCV:
RCV002305300
ClinVar Variation:
1721533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006352.2:p.Val269Leu
CA400105547
NM_006361.6:c.805G>C