Canonical Allele Identifier: PA2825799858
Gene: CNGA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087458
ClinVar RCV Id: RCV003017856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136036.2:p.Ser544Arg
CA356824798
NM_001142564.2:c.1632C>G
CA356824800
NM_001142564.2:c.1632C>A
CA356824806
NM_001142564.2:c.1630A>C