Canonical Allele Identifier: PA916011457
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491936
ClinVar RCV Id: RCV000582599 RCV000708887 RCV000807532 RCV003459447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Phe973Val
CA346758568
NM_001281492.2:c.2917T>G