Canonical Allele Identifier: PA916013544
Gene: CAD HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004332.2:p.Phe1644Leu
CA1573698
NM_004341.4:c.4930T>C
CA346221760
NM_004341.4:c.4932C>G
CA346221761
NM_004341.4:c.4932C>A