Canonical Allele Identifier: PA645381248
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230544
ClinVar Variation Id: 965508
ClinVar RCV Id: RCV001239977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val653Leu
CA068319
NM_000179.3:c.1957G>C
CA46710015
NM_000179.3:c.1957G>T