Allele Registry

Canonical Allele Identifier: PA288229

Gene: HOXB13 HGNC NCBI

ClinVar RCV:

RCV000115970

RCV001020842

ClinVar Variation:

128032

HGVS (amino-acid)	Matching Registered Transcripts
NP_006352.2:p.Ser122Arg	CA288227 NM_006361.6:c.366C>A CA400107610 NM_006361.6:c.366C>G CA400107613 NM_006361.6:c.364A>C