Canonical Allele Identifier: PA174733
Gene: ABCG4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161759
ClinVar RCV Id: RCV000149295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071452.2:p.Arg79Ser
CA174732
NM_022169.5:c.237G>T
CA6315897
NM_022169.5:c.237G>C