Canonical Allele Identifier: PA261359
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42948
ClinVar RCV Id: RCV000629019 RCV001188088 RCV001258092 RCV001703459 RCV002321503 RCV002496541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1045Leu
CA013375
NM_000257.4:c.3134G>T