Canonical Allele Identifier: PA645379918
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 336442
ClinVar RCV Id: RCV000300787 RCV000688085 RCV000564277 RCV001571224 RCV003995876
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu423Ile
CA10615505
NM_000179.3:c.1267C>A