Canonical Allele Identifier: PA2829761470
Gene: AMACR HGNC NCBI

Linked Data

ClinVar Variation Id: 2193469
ClinVar RCV Id: RCV002608002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055139.4:p.Gly13Arg
CA3226307
NM_014324.6:c.37G>C