Canonical Allele Identifier: PA1139674279
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 835697
ClinVar RCV Id: RCV001036642 RCV001585935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1337Pro
CA389041237
NM_000257.4:c.4010G>C