Allele Registry

Canonical Allele Identifier: PA2827312276

Gene: RHCE HGNC NCBI

ClinVar RCV:

RCV000144442

ClinVar Variation:

156358

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317359.1:p.Pro103Ser	CA233211 NM_001330430.4:c.307C>T