Canonical Allele Identifier: PA2828936739
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948931
ClinVar RCV Id: RCV001220288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001371071.1:p.Pro665Ala
CA5247222
NM_001384142.1:c.1993C>G