Canonical Allele Identifier: PA2826036279
Gene: AMACR HGNC NCBI

Linked Data

ClinVar Variation Id: 501618
ClinVar RCV Id: RCV000594793 RCV001333042 RCV003935621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161067.1:p.Pro37Thr
CA3226294
NM_001167595.2:c.109C>A