Allele Registry

Canonical Allele Identifier: PA096745

Gene: HCRT HGNC NCBI

ClinVar RCV:

RCV000007726

ClinVar Variation:

7303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001515.1:p.Leu16Arg	CA118704 NM_001524.1:c.47T>G