Canonical Allele Identifier: PA1139672672
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 927069
ClinVar RCV Id: RCV001190080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met303Val
CA346740712
NM_000179.3:c.907A>G