Canonical Allele Identifier: PA2580336602
Gene: SRSF5 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008856.2:p.Asn272Asp
CA7245825
NM_006925.5:c.814A>G