Canonical Allele Identifier: PA915961047
Gene: SLC12A3 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000330.3:p.Arg871His
CA032037
NM_000339.3:c.2612G>A