Canonical Allele Identifier: PA645416960
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 312900
ClinVar RCV Id: RCV000281839 RCV000330935 RCV000363030 RCV000385552 RCV001540354 RCV001525477 RCV002522300 RCV003320160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1325Val
CA039802
NM_000257.4:c.3974C>T