Canonical Allele Identifier: PA2827065163
Gene: SEPTIN10 HGNC NCBI

Linked Data

ClinVar Variation Id: 3160031
ClinVar RCV Id: RCV004452933
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308436.1:p.Val41Leu
CA1826292
NM_001321507.2:c.121G>T
CA348067689
NM_001321507.2:c.121G>C