Canonical Allele Identifier: PA2826630788
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182626
ClinVar RCV Id: RCV000196510 RCV000491442 RCV000589796 RCV000757926 RCV002271428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile306Val
CA009270
NM_001281493.2:c.916A>G