Canonical Allele Identifier: PA174431
Gene: S100A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 161603
ClinVar RCV Id: RCV000149139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002951.1:p.Val9Leu
CA174430
NM_002960.1:c.25G>T
CA342526905
NM_002960.1:c.25G>C