Allele Registry

Canonical Allele Identifier: PA035928

Gene: HBG1 HGNC NCBI

ClinVar RCV:

RCV002227183

ClinVar Variation:

478899

HGVS (amino-acid)	Matching Registered Transcripts
NP_000550.2:p.Ala137Gly	CA035916 NM_000559.3:c.410C>G CA035937 NM_000559.3:c.[410C>G;227C>T]