Canonical Allele Identifier: PA287326
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127594
ClinVar RCV Id: RCV000115424 RCV000119134 RCV000410495 RCV000656904 RCV001194392 RCV001354737
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Cys1275Tyr
CA014456
NM_000179.3:c.3824G>A