Canonical Allele Identifier: PA2826623136
Gene: RCC1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2347900
ClinVar RCV Id: RCV004182532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268370.1:p.Thr152Met
CA4299073
NM_001281441.2:c.455C>T