Canonical Allele Identifier: PA2828936559
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413339
ClinVar RCV Id: RCV001925865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371071.1:p.Leu413Phe
CA5246899
NM_001384142.1:c.1239G>T
CA374932514
NM_001384142.1:c.1239G>C