Canonical Allele Identifier: PA144629
Gene: ANO5 HGNC NCBI

Linked Data

ClinVar Variation Id: 60689
ClinVar RCV Id: RCV000054502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136121.1:p.Thr513Ile
CA144627
NM_001142649.2:c.1538C>T