Canonical Allele Identifier: PA645485776
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 345326
ClinVar RCV Id: RCV000270617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_877437.2:p.Ala60Val
CA10618843
NM_182760.4:c.179C>T