Canonical Allele Identifier: PA2826631027
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713432
ClinVar RCV Id: RCV002295462 RCV002416562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Met360Arg
CA346750635
NM_001281493.2:c.1079T>G