Canonical Allele Identifier: PA2825544864
Gene: PACS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365709
ClinVar RCV Id: RCV001929933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001094383.2:p.Pro35Thr
CA391191901
NM_001100913.3:c.103C>A