Canonical Allele Identifier: PA658746393
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 495707
ClinVar RCV Id: RCV000587268 RCV000772486 RCV000821395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln776His
CA346753318
NM_000179.3:c.2328A>C
CA346753321
NM_000179.3:c.2328A>T