Canonical Allele Identifier: PA2828749660
Gene: UMOD HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365162.1:p.Cys315Arg
CA256254
NM_001378233.1:c.943T>C