Canonical Allele Identifier: PA2580117078
Gene: TM6SF2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2409714
ClinVar RCV Id: RCV004246740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001524.2:p.Val301Leu
CA9324632
NM_001001524.3:c.901G>T
CA404924482
NM_001001524.3:c.901G>C