Canonical Allele Identifier: PA132129
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43098
ClinVar RCV Id: RCV000157351 RCV000158879 RCV000223687 RCV000252658 RCV000811971 RCV000852457 RCV001265607 RCV001823103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg237Trp
CA016662
NM_000257.4:c.709C>T