Canonical Allele Identifier: PA2826131994
Gene: SAA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2309057
ClinVar RCV Id: RCV004160016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171477.2:p.Trp103Cys
CA379506309
NM_001178006.3:c.309G>C
CA379506311
NM_001178006.3:c.309G>T