Canonical Allele Identifier: PA2573062044
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315927
ClinVar RCV Id: RCV001757374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1046Leu
CA389045421
NM_000257.4:c.3136A>C
CA389045422
NM_000257.4:c.3136A>T