Canonical Allele Identifier: PA214530
Gene: CHGB HGNC NCBI

Linked Data

ClinVar Variation Id: 161584
ClinVar RCV Id: RCV000149119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001810.2:p.Glu436Asp
CA214529
NM_001819.3:c.1308A>C
CA408186958
NM_001819.3:c.1308A>T