Canonical Allele Identifier: PA891850750
Gene: LAS1L HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_112483.1:p.Arg401Ser
CA413317256
NM_031206.7:c.1203G>T
CA413317257
NM_031206.7:c.1203G>C