Canonical Allele Identifier: PA296666
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181254
ClinVar RCV Id: RCV000158653 RCV000466942 RCV001180570 RCV004019918 RCV003998361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1434Cys
CA014792
NM_000257.4:c.4300C>T