Canonical Allele Identifier: PA2573074916
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 253010
ClinVar RCV Id: RCV001233689 RCV002251340
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.Asp607Glu
CA7939065
NM_001378235.1:c.1821C>G
CA394980986
NM_001378235.1:c.1821C>A