Allele Registry

Canonical Allele Identifier: PA107785

Gene: HAMP HGNC NCBI

ClinVar RCV:

RCV000004507

RCV000599701

RCV000990194

RCV001086432

RCV001127434

RCV003974795

ClinVar Variation:

4286

HGVS (amino-acid)	Matching Registered Transcripts
NP_066998.1:p.Gly71Asp	CA340226 NM_021175.4:c.212G>A