Canonical Allele Identifier: PA2826626968
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525592
ClinVar RCV Id: RCV000629678 RCV000774601 RCV004002769
ClinVar Variation Id: 839817
ClinVar RCV Id: RCV001041663
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr597Ser
CA068566
NM_001281492.2:c.1790C>G
CA346751208
NM_001281492.2:c.1789A>T