Canonical Allele Identifier: PA2827196097
Gene: SUPV3L1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001310513.1:p.Leu527Val
CA376911563
NM_001323584.2:c.1579C>G