Canonical Allele Identifier: PA2825912751
Gene: LRRC36 HGNC NCBI

Linked Data

ClinVar Variation Id: 2623468
ClinVar RCV Id: RCV004364178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155047.1:p.Ser380Phe
CA8109721
NM_001161575.1:c.1139C>T