Canonical Allele Identifier: PA2580544252
Gene: LRATD2 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_777571.1:p.Val181Met
CA372274731
NM_174911.5:c.541G>A