Canonical Allele Identifier: PA132040
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43041
ClinVar RCV Id: RCV000035935 RCV000456855 RCV000767039 RCV003996214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1613Lys
CA015403
NM_000257.4:c.4838G>A