Canonical Allele Identifier: PA1139673355
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 843363
ClinVar RCV Id: RCV001045971 RCV002393226
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val508Met
CA067797
NM_000179.3:c.1522G>A