Canonical Allele Identifier: PA2826629005
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127594
ClinVar RCV Id: RCV000115424 RCV000119134 RCV000410495 RCV000656904 RCV001194392 RCV001354737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Cys1145Tyr
CA014456
NM_001281492.2:c.3434G>A