Canonical Allele Identifier: PA2573166278
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477833
ClinVar RCV Id: RCV001971787

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe230Leu
CA389052250
NM_000257.4:c.690T>G
CA389052251
NM_000257.4:c.690T>A
CA389052255
NM_000257.4:c.688T>C