Canonical Allele Identifier: PA2826628568
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230554
ClinVar RCV Id: RCV004520705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile1053Leu
CA346760258
NM_001281492.2:c.3157A>C
CA346760260
NM_001281492.2:c.3157A>T