Canonical Allele Identifier: PA645384173
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410454
ClinVar RCV Id: RCV000775741 RCV000465628 RCV004001834
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly1186Arg
CA16610969
NM_000179.3:c.3556G>C