Canonical Allele Identifier: PA299439
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182625
ClinVar RCV Id: RCV000160670 RCV000545304 RCV000774598 RCV000781596 RCV003998493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val586Ala
CA009128
NM_000179.3:c.1757T>C