Canonical Allele Identifier: PA2573185015
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1441676
ClinVar RCV Id: RCV001967986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Met318Leu
CA375368693
NM_001162426.2:c.952A>T
CA375368695
NM_001162426.2:c.952A>C