Canonical Allele Identifier: PA131865
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42919
ClinVar RCV Id: RCV000035809 RCV002426555 RCV001347585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu875del
CA012755
NM_000257.4:c.2623_2625del
CA389047976
NM_000257.4:c.2623G>T
CA389047984
NM_000257.4:c.2620G>T