Canonical Allele Identifier: PA2825842358
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2622552
ClinVar RCV Id: RCV003381691
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Val262Leu
CA362452563
NM_001142298.2:c.784G>T
CA362452565
NM_001142298.2:c.784G>C