Canonical Allele Identifier: PA2825109077
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1759485
ClinVar RCV Id: RCV002393985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe252Leu
CA389052116
NM_000257.4:c.756T>A
CA389052117
NM_000257.4:c.756T>G
CA389052120
NM_000257.4:c.754T>C