Canonical Allele Identifier: PA2828437498
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3153440
ClinVar RCV Id: RCV004446341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357463.1:p.Ser408Gly
CA396762182
NM_001370534.1:c.1222A>G