Canonical Allele Identifier: PA2826633013
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 644510
ClinVar RCV Id: RCV000798446 RCV002458443 RCV002271586 RCV003442082
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu819Asp
CA070730
NM_001281493.2:c.2457G>C
CA346758783
NM_001281493.2:c.2457G>T