Canonical Allele Identifier: PA645394515
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 408267
ClinVar RCV Id: RCV000468628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612370.3:p.Cys694Arg
CA5247259
NM_138361.5:c.2080T>C