Canonical Allele Identifier: PA913193996
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 619082
ClinVar RCV Id: RCV000757956 RCV001207953 RCV002343609 RCV003333104 RCV003333106 RCV003150341 RCV003333107 RCV003333103 RCV003333105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly181Arg
CA046725
NM_000257.4:c.541G>A
CA389052585
NM_000257.4:c.541G>C