Allele Registry

Canonical Allele Identifier: PA114919

Gene: SLC4A11 HGNC NCBI

ClinVar RCV:

RCV000001378

ClinVar Variation:

1315

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167560.1:p.Met840Val	CA114918 NM_001174089.2:c.2518A>G