Canonical Allele Identifier: PA2826142496
Gene: HADH HGNC NCBI

Linked Data

ClinVar Variation Id: 211127
ClinVar RCV Id: RCV000194877 RCV000757347 RCV000764522 RCV001086439 RCV001143929 RCV000664100 RCV003907686
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171634.3:p.Gln152His
CA209330
NM_001184705.4:c.456G>T
CA357832852
NM_001184705.4:c.456G>C