Canonical Allele Identifier: PA2828750273
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 3066261
ClinVar RCV Id: RCV003991265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Cys256Ser
CA394984597
NM_001378235.1:c.767G>C
CA394984613
NM_001378235.1:c.766T>A