Allele Registry

Canonical Allele Identifier: PA094856

Gene: SLC40A1 HGNC NCBI

ClinVar RCV:

RCV001858656

ClinVar Variation:

801843

HGVS (amino-acid)	Matching Registered Transcripts
NP_055400.1:p.Asn144Asp	CA349989223 NM_014585.6:c.430A>G