Canonical Allele Identifier: PA658681034
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479929
ClinVar RCV Id: RCV000570721 RCV000588628 RCV000692110 RCV001821659 RCV003459291 RCV004000882
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met868Ile
CA069280
NM_000179.3:c.2604G>A
CA346754948
NM_000179.3:c.2604G>C
CA346754949
NM_000179.3:c.2604G>T