Canonical Allele Identifier: PA296652
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181246
ClinVar RCV Id: RCV000158640 RCV000823777 RCV001804875 RCV003362698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1396Trp
CA014576
NM_000257.4:c.4186C>T