Canonical Allele Identifier: PA658804477
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 518874
ClinVar RCV Id: RCV000620889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe856Leu
CA389048133
NM_000257.4:c.2568C>G
CA389048134
NM_000257.4:c.2568C>A
CA389048139
NM_000257.4:c.2566T>C