Canonical Allele Identifier: PA131946
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42978
ClinVar RCV Id: RCV000035871 RCV000628955 RCV001198766 RCV001525525 RCV004018776 RCV003129764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1286Lys
CA014172
NM_000257.4:c.3856G>A