Canonical Allele Identifier: PA2828750301
Gene: UMOD HGNC NCBI

Linked Data

ClinVar Variation Id: 1953992
ClinVar RCV Id: RCV002714921
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365164.1:p.His314Gln
CA394983718
NM_001378235.1:c.942C>A
CA394983719
NM_001378235.1:c.942C>G