Canonical Allele Identifier: PA2826628539
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410425
ClinVar RCV Id: RCV000521217 RCV000469909 RCV000568727 RCV000663017 RCV003463928 RCV004001826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu1047Val
CA071122
NM_001281492.2:c.3139C>G