Allele Registry

Canonical Allele Identifier: PA151764

Gene: AMACR HGNC NCBI

ClinVar RCV:

RCV000116322

RCV000276161

RCV000676067

RCV001049000

RCV001549128

ClinVar Variation:

128358

845848

HGVS (amino-acid)	Matching Registered Transcripts
NP_055139.4:p.Leu201Ser	CA151762 NM_014324.6:c.602T>C CA916082696 NM_014324.6:c.602_603delinsCA