Canonical Allele Identifier: PA2829447350
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1348894
ClinVar RCV Id: RCV002035076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003352.2:p.Cys300Ser
CA394983876
NM_003361.4:c.899G>C
CA394983878
NM_003361.4:c.898T>A