Canonical Allele Identifier: PA2825924479
Gene: MBOAT7 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139528.1:p.Val238Met
CA309346273
NM_001146056.3:c.712G>A