Canonical Allele Identifier: PA2826635560
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025897
ClinVar RCV Id: RCV001326274 RCV001525365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Met360Lys
CA346750633
NM_001281494.2:c.1079T>A