Allele Registry

Canonical Allele Identifier: PA916069686

Gene: RHCE HGNC NCBI

ClinVar RCV:

RCV000144442

ClinVar Variation:

156358

HGVS (amino-acid)	Matching Registered Transcripts
NP_619524.5:p.Pro103Ser	CA233211 NM_138618.6:c.307C>T