Canonical Allele Identifier: PA916010914
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 216318
ClinVar RCV Id: RCV000196789 RCV000575547 RCV000662898 RCV001564528 RCV003462323 RCV003150088 RCV003997002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser14Phe
CA336718
NM_001281492.2:c.41C>T