Canonical Allele Identifier: PA2828060378
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 48896
ClinVar RCV Id: RCV000042147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Gln580His
CA006014
NM_001362177.1:c.1740G>T
CA375361047
NM_001362177.1:c.1740G>C