Canonical Allele Identifier: PA106568
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2672
ClinVar RCV Id: RCV000002791 RCV000082715
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_877437.2:p.Ser155Pro
CA115675
NM_182760.4:c.463T>C