Canonical Allele Identifier: PA2828749229
Gene: UMOD HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Cys126Arg
CA256246
NM_001378232.1:c.376T>C