Canonical Allele Identifier: PA2828749333
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1348894
ClinVar RCV Id: RCV002035076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365161.1:p.Cys300Ser
CA394983876
NM_001378232.1:c.899G>C
CA394983878
NM_001378232.1:c.898T>A