Canonical Allele Identifier: PA2829935477
Gene: RHCE HGNC NCBI

Linked Data

ClinVar Variation Id: 156358
ClinVar RCV Id: RCV000144442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065231.4:p.Pro103Ser
CA233211
NM_020485.8:c.307C>T