Allele Registry

Canonical Allele Identifier: PA124723

Gene: HBB HGNC NCBI

ClinVar Allele:

30134

ClinVar RCV:

RCV000016248

ClinVar Variation:

15095

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala136Pro	CA124722 NM_000518.5:c.406G>C