Canonical Allele Identifier: PA2741903412
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2622552
ClinVar RCV Id: RCV003381691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Val346Leu
CA362452563
NM_003900.5:c.1036G>T
CA362452565
NM_003900.5:c.1036G>C