Canonical Allele Identifier: PA098781
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181319
ClinVar RCV Id: RCV000158757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe244Leu
CA016711
NM_000257.4:c.730T>C
CA389052169
NM_000257.4:c.732C>G
CA389052170
NM_000257.4:c.732C>A
CA2695219147
NM_000257.4:c.730_732delinsCTT