Canonical Allele Identifier: PA2826631397
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483771
ClinVar RCV Id: RCV000566523 RCV000823922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly447Val
CA346752639
NM_001281493.2:c.1340G>T