Canonical Allele Identifier: PA658675414
Gene: ACADVL HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000009.1:p.Cys607Ser
CA8338274
NM_000018.4:c.1820G>C
CA397725958
NM_000018.4:c.1819T>A