Canonical Allele Identifier: PA2825925062
Gene: MBOAT7 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139554.1:p.Val311Met
CA309346273
NM_001146082.3:c.931G>A