Canonical Allele Identifier: PA2827509499
Gene: MECR HGNC NCBI

Linked Data

ClinVar Variation Id: 2175054
ClinVar RCV Id: RCV002602231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336640.1:p.Asp276Glu
CA725531
NM_001349711.2:c.828C>G
CA339537035
NM_001349711.2:c.828C>A