Canonical Allele Identifier: PA258172
Gene: ASCL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18332
ClinVar RCV Id: RCV000019998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004307.2:p.Pro18Thr
CA258171
NM_004316.4:c.52C>A