Canonical Allele Identifier: PA180680
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177741
ClinVar RCV Id: RCV000154353 RCV000172568 RCV000629143 RCV001112127 RCV001111654 RCV001111655 RCV003320109 RCV001171226 RCV004019847
ClinVar Variation Id: 180057
ClinVar RCV Id: RCV000156860 RCV001171227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly10Arg
CA013184
NM_000257.4:c.28G>A
CA013193
NM_000257.4:c.28G>C