Canonical Allele Identifier: PA1139674397
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 921312
ClinVar RCV Id: RCV001180660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys660Arg
CA346750621
NM_000179.3:c.1979A>G