Canonical Allele Identifier: PA2830288658
Gene: RCC1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2347900
ClinVar RCV Id: RCV004182532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683682.1:p.Thr152Met
CA4299073
NM_148842.2:c.455C>T