Canonical Allele Identifier: PA2825092083
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 849724
ClinVar RCV Id: RCV001053749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val1231Ala
CA346760964
NM_000179.3:c.3692T>C