Canonical Allele Identifier: PA106465
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2669
ClinVar RCV Id: RCV000002788 RCV000082716
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_877437.2:p.Ala279Val
CA115674
NM_182760.4:c.836C>T