Canonical Allele Identifier: PA2825091278
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171608
ClinVar RCV Id: RCV001524841 RCV001872052
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1127Val
CA346758821
NM_000179.3:c.3380C>T