Allele Registry

Canonical Allele Identifier: PA151766

Gene: AMACR HGNC NCBI

ClinVar RCV:

RCV000116323

RCV000306332

RCV000676065

ClinVar Variation:

128359

HGVS (amino-acid)	Matching Registered Transcripts
NP_055139.4:p.Gln239His	CA151765 NM_014324.6:c.717G>T CA359381188 NM_014324.6:c.717G>C