Allele Registry

Canonical Allele Identifier: PA124678

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016218

ClinVar Variation:

15067

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Asp48Val	CA124677 NM_000519.4:c.143A>T