Canonical Allele Identifier: PA2826633622
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 134856
ClinVar RCV Id: RCV000121589 RCV000160698 RCV000206271 RCV000411602 RCV000656902 RCV003460856 RCV003997354
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Val951Ala
CA014193
NM_001281493.2:c.2852T>C