Canonical Allele Identifier: PA299485
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89443
ClinVar RCV Id: RCV000160696 RCV000212686 RCV000410774 RCV000524182 RCV000780485 RCV001354592 RCV003153344 RCV003460688 RCV003997095
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1225Met
CA013768
NM_000179.3:c.3674C>T