Canonical Allele Identifier: PA1139674310
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 919055
ClinVar RCV Id: RCV001176981 RCV002558837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1360Asp
CA389041002
NM_000257.4:c.4079T>A