Canonical Allele Identifier: PA2826908235
Gene: CAD HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293008.1:p.Phe1581Leu
CA1573698
NM_001306079.2:c.4741T>C
CA346221760
NM_001306079.2:c.4743C>G
CA346221761
NM_001306079.2:c.4743C>A