Canonical Allele Identifier: PA2826630476
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142272
ClinVar RCV Id: RCV000131295 RCV000693545 RCV003998099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser234Asn
CA008866
NM_001281493.2:c.701G>A