Canonical Allele Identifier: PA2826036280
Gene: AMACR HGNC NCBI

Linked Data

ClinVar Variation Id: 1405520
ClinVar RCV Id: RCV001935194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161067.1:p.Ser39Phe
CA359385302
NM_001167595.2:c.116C>T