Canonical Allele Identifier: PA916069529
Gene: AMACR HGNC NCBI

Linked Data

ClinVar Variation Id: 501618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_976316.1:p.Pro37Thr
CA3226294
NM_203382.3:c.109C>A