Canonical Allele Identifier: PA2825268098
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 365031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005373.1:p.Ala591Val
CA5247123
NM_001005373.4:c.1772C>T