Canonical Allele Identifier: PA2826632854
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525751
ClinVar RCV Id: RCV000630015 RCV000771661 RCV003332215 RCV004002789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Pro784Ser
CA346758131
NM_001281493.2:c.2350C>T