Canonical Allele Identifier: PA2826632818
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134855
ClinVar RCV Id: RCV000121586 RCV000214188 RCV000200854 RCV000590417 RCV003997353 RCV000663151 RCV003460855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val776Ala
CA012103
NM_001281493.2:c.2327T>C