Canonical Allele Identifier: PA2826864657
Gene: SUPV3L1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288612.1:p.Ile195Val
CA209214824
NM_001301683.2:c.583A>G